DNA Traits · Appearance
Finger length ratio (SALL1 marker)
The length of the index finger compared with the ring finger.

What the research found
In the cited research, the A allele at rs6499762 was associated with a higher index to ring finger length ratio.
- CC
- Lower ratio
- AC
- Middle
- AA
- Higher ratio
What the study found
In the study, each copy went with index finger length as a percentage of ring finger length, left hand about 0.44 ratio points higher on average.
- Evidence
- Genome-wide association with independent replication
- Who was studied
- European ancestry cohorts from the UK, the Netherlands and Australia; replicated in 23andMe research participants
How common each genotype is
| Region | CCLower ratio | ACMiddle | AAHigher ratio |
|---|---|---|---|
| All regions2,504 people | 73% | 24% | 2% |
| Africa661 people | 69% | 28% | 3% |
| The Americas347 people | 84% | 16% | <1% |
| East Asia504 people | 85% | 14% | <1% |
| Europe503 people | 75% | 23% | 1% |
| South Asia489 people | 57% | 37% | 6% |
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 | 16%19 of 118 copies read |
|---|---|
| First farmers6500 to 3000 BC | 15%180 of 1,175 copies read |
| Bronze Age3000 to 1200 BC | 12%145 of 1,169 copies read |
| Iron Age and Antiquity1200 BC to AD 600 | 13%226 of 1,714 copies read |
| Middle AgesAD 600 to 1500 | 13%191 of 1,484 copies read |
| Today1000 Genomes | 13%131 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
- SALL1 region
- Marker
- rs6499762
- Location
- Chromosome 16 · GRCh37 51,697,874 · GRCh38 51,663,963
- Letters studied
- A and C, 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
- SALL1 region · rs6499762
- Location
- Chromosome 16 · GRCh37 51,697,874 · GRCh38 51,663,963
- Studied allele
- A
- Published statistic
- beta 0.441 (SE 0.056) per A allele on 2D:4D x 100, P 5.33e-15, EAF 0.125 (Table 2, European discovery meta-analysis); 23andMe replication beta 0.083 (SE 0.006) on a three-level self-reported finger-length scale, P 2.83e-41, n 75,821 (Table 2); same direction in all six discovery cohorts, heterogeneity P 0.221 (Supplementary Table S3); the lead SNPs at the 12 replicated signals together explain 3.8% of the variance (Results) (Table 2 (rs6499762, discovery row); Supplementary Table S3; Discussion (European-only left-hand analysis, N 14 382))
- 1000 Genomes Project phase 3, people with 0, 1 and 2 copies
- All regions 1836 / 608 / 60 · Africa 456 / 186 / 19 · The Americas 291 / 55 / 1 · East Asia 430 / 71 / 3 · Europe 379 / 117 / 7 · South Asia 280 / 179 / 30
What it cannot tell you
A single marker, one of many that shape finger proportions. Measured on the left hand.
Genome-wide association study identifies nine novel loci for 2D:4D finger ratio, a putative retrospective biomarker of testosterone exposure in utero (Warrington et al., 2018)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
- 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 (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.