DNA Traits · Appearance
Nose bridge breadth association
How broad the bridge of the nose is, between the eyes.

What the research found
In the cited research, the T allele at rs1852985 was associated with greater nose bridge breadth in the studied cohorts.
- CC
- Narrower
- CT
- Middle
- TT
- Broader
What the study found
In the study, each copy went with nose bridge breadth rating from photos, on a three level scale where higher is broader about 0.07 points higher on average.
- Evidence
- Genome-wide association with independent replication
- Who was studied
- Admixed Latin American CANDELA participants from Brazil, Chile, Colombia, Mexico and Peru
How common each genotype is
| Region | CCNarrower | CTMiddle | TTBroader |
|---|---|---|---|
| All regions2,504 people | 68% | 28% | 4% |
| Africa661 people | 70% | 27% | 3% |
| The Americas347 people | 56% | 34% | 10% |
| East Asia504 people | 57% | 37% | 6% |
| Europe503 people | 76% | 23% | 1% |
| South Asia489 people | 79% | 20% | 2% |
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.
The marker
- Gene or region
- SUPT3H / RUNX2 region
- Marker
- rs1852985
- Location
- Chromosome 6 · GRCh37 45,329,656 · GRCh38 45,361,919
- Letters studied
- C and T, with T 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
- SUPT3H / RUNX2 region · rs1852985
- Location
- Chromosome 6 · GRCh37 45,329,656 · GRCh38 45,361,919
- Studied allele
- T
- Published statistic
- effect 0.069 per T allele on the ordinal rating, P 6e-10, 0.71% of variance, n 5,958; independent replication P 5e-3 in 501 people (Table 1); quantitative follow-up effect 4.4e-4 (Procrustes-scaled landmark distance), P 2e-8, 1.18% of variance, n 2,955 (Table 2) (Table 1; Supplementary Figure 1 (three levels coded 0 to 2))
- 1000 Genomes Project phase 3, people with 0, 1 and 2 copies
- All regions 1710 / 694 / 100 · Africa 460 / 178 / 23 · The Americas 196 / 117 / 34 · East Asia 289 / 187 / 28 · Europe 380 / 116 / 7 · South Asia 385 / 96 / 8
What it cannot tell you
This small marker association concerns measured facial geometry in the research sample. It does not reconstruct your face, classify attractiveness or calculate a facial measurement. Only the studied C/T allele pair is interpreted.
A genome-wide association scan implicates DCHS2, RUNX2, GLI3, PAX1 and EDAR in human facial variation (Adhikari et al., 2016)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 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 (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.