DNA Traits · Appearance
Male pattern hair loss
How much scalp hair men lose in the usual male pattern, from a receding hairline to a thinning crown.

What the research found
In the cited research, the A allele at rs1160312 was associated with more extensive male pattern hair loss in the studied men.
- GG
- Less balding
- AG
- Middle
- AA
- More balding
What the study found
In the study, each copy went with self-reported hair loss pattern on a four step scale from no balding to extensive balding, adjusted for age and ancestry about 0.15 points higher on average.
- Evidence
- Genome-wide association with independent replication
- Who was studied
- Men of European ancestry
The research behind this card was done only in men, so it is part of a report requested as male.
How common each genotype is
| Region | GGLess balding | AGMiddle | AAMore balding |
|---|---|---|---|
| All regions2,504 people | 41% | 43% | 16% |
| Africa661 people | 53% | 40% | 7% |
| The Americas347 people | 49% | 40% | 11% |
| East Asia504 people | 48% | 40% | 13% |
| Europe503 people | 25% | 44% | 31% |
| South Asia489 people | 27% | 51% | 21% |
Among the 2,504 people of the 1000 Genomes Project, in five world regions. These percentages describe groups of people, never anyone’s chance of having a trait.
Through time
How often the studied letter was read in ancient people, era by era, in the region chosen.
| Before farmingbefore 6500 BC | 46%30 of 65 copies read |
|---|---|
| First farmers6500 to 3000 BC | 45%411 of 921 copies read |
| Bronze Age3000 to 1200 BC | 46%397 of 854 copies read |
| Iron Age and Antiquity1200 BC to AD 600 | 45%495 of 1,099 copies read |
| Middle AgesAD 600 to 1500 | 47%245 of 523 copies read |
| Today1000 Genomes | 53%534 of 1,006 copies |
Neanderthal and Denisovan genomes
- Altai Neanderthal
- No copies
- Vindija Neanderthal
- No copies
- Chagyrskaya Neanderthal
- No copies
- Denisovan
- No copies
Neanderthals and Denisovans carried the other letter, so this letter is younger than our split with them.
The marker
- Gene or region
- 20p11.22 region between PAX1 and FOXA2
- Marker
- rs1160312
- Location
- Chromosome 20 · GRCh37 22,050,503 · GRCh38 22,069,865
- Letters studied
- A and G, with A as the studied allele
A DNA Traits report reads this marker in your raw DNA file and shows which of the three genotypes is yours, with how common it is. It counts the copies of the studied allele; it does not measure the trait itself.
- Marker
- 20p11.22 region between PAX1 and FOXA2 · rs1160312
- Location
- Chromosome 20 · GRCh37 22,050,503 · GRCh38 22,069,865
- Studied allele
- A
- Published statistic
- Discovery: OR 1.79 (1.49 to 2.15) per A, P 3.2e-10, CoLaus extreme case-control study of 578 early-onset cases and 547 controls; replication OR 1.68 TwinsUK (P 2.0e-3), 1.41 Iceland (P 6.1e-3), 1.40 Netherlands (P 0.018); all men OR 1.60 (1.42 to 1.80), P 1.1e-14 (Richards 2008 Table 1). UK Biobank: 0.149 points per A on the adjusted four-pattern score (SE 0.003, n 205,327; Yap 2018 Supplementary Data 3); log-odds 0.337 per A (SE 0.017), P 3.4e-87 in Pirastu's replication cohorts (Pirastu 2017 Supplementary Data 2) (Supplementary Data 3 (rs1160312 row: ALLELE1 G, A1FREQ 0.457, BETA -0.1488, SE 0.0031, P printed as 0) and Results (scores 1 to 4, adjusted for age, assessment centre, ethnicity and 40 principal components))
- 1000 Genomes Project phase 3, people with 0, 1 and 2 copies
- All regions 1017 / 1078 / 409 · Africa 350 / 266 / 45 · The Americas 169 / 139 / 39 · East Asia 240 / 200 / 64 · Europe 125 / 222 / 156 · South Asia 133 / 251 / 105
What it cannot tell you
Studied in men of European ancestry. One of hundreds of markers that shape male pattern hair loss.
Male-pattern baldness susceptibility locus at 20p11 (Richards et al., 2008)More in Appearance
- Eye pigmentation
- Red hair association
- Blond hair association
- Hair shape
- Hair thickness association
- Skin pigmentation
- Freckling association
- Hair greying association
- Eyebrow thickness association
- Beard density association
- Unibrow association
- Nose bridge breadth association
- Nose wing breadth association
- Nose protrusion association
- Nose tip angle association
- Chin protrusion association
- Earlobe attachment association
- Earlobe size association
- Ear ridge folding association
- Male pattern hair loss, HDAC9 marker
- Male pattern hair loss, EBF1 marker
- Male pattern hair loss, WNT10A marker
- Hair lightness, SLC24A4 marker
- Blond hair, TPCN2 marker
- Hair lightness, SLC45A2 marker
- Red hair, ASIP region marker
- Hair lightness, HERC2 marker
- Hair colour, IRF4 marker
- Hair shape, WNT10A marker
- Hair shape, PADI3 marker
- Hair shape, HOXC13 marker
- Hair shape, GATA3 region marker
- Hair shape, FRAS1 marker
- Hair shape, LCE3E marker
- Straight hair, EDAR marker
- Eyebrow thickness, FOXD1 region marker
- Eyebrow thickness, FOXL2 marker
- Shovel-shaped incisors
- Finger length ratio (SMOC1 marker)
- Finger length ratio (LDAH marker)
- Finger length ratio (SALL1 marker)
- Finger length ratio (OLA1 marker)
- Nose root position
- Nose wing breadth (PAX1 marker)
- Earlobe attachment (PAX9 marker)
- Earlobe attachment (KIAA1217 marker)
- Earlobe attachment (MRPS22 marker)
- Fingerprint whorls (ADAMTS9 marker)
- Fingerprint whorls (EVI1 marker)
- Fingerprint whorls (SALL3 marker)
- Green or hazel eyes
- Eye pigmentation (TYR)
- Freckling (TYR)
- Skin pigmentation (OCA2 H615R)
- Freckling (PPARGC1B)
- Freckling (HSPA12A)
- Freckling (BNC2)
- Freckling (EMX2)
- Freckling (EIF6, ASIP region)
- Skin lightness (OCA2 A481T)
- Eye pigmentation (TSPAN10)
- Eye pigmentation (TYRP1)
- Eye pigmentation (SLC24A4)
- Eye pigmentation (SIK1)
- Eye pigmentation (OCA2 exon ten)
See your own two letters.
Upload the raw DNA file you already have. Your report reads this marker and every other card studied for you, each with its evidence and its limits.