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DNA Traits · Appearance

Hair shape, FRAS1 marker

Whether scalp hair grows straight, wavy or curly.

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Evidence · Replicated

What the research found

In the cited research, the T allele at rs1268789 was associated with curlier scalp hair.

CC
Straighter
CT
Middle
TT
Curlier
Slight effect

What the study found

In the study, each copy went with hair curliness on a three level scale from straight through wavy to curly about 0.09 points higher on average.

US volunteers, 98% of European ancestry (US sample) · 743 people · Supplementary Table 2 (rs1268789 row, US column: frequency 0.317, beta 0.0865, SE 0.0350, P 0.014) and Methods (US three level curliness scale)
Evidence
Replicated genome-wide association
Who was studied
Primarily European ancestry
1000 Genomes Project

How common each genotype is

How common each genotype is in the 1000 Genomes Project, by region
RegionCCStraighterCTMiddleTTCurlier
All regions2,504 people32%44%24%
Africa661 people47%44%9%
The Americas347 people44%44%12%
East Asia504 people6%39%55%
Europe503 people44%45%12%
South Asia489 people20%47%33%

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.

Ancient genomes

Through time

How often the studied letter was read in ancient people, era by era, in the region chosen.

Region
Through time: Europe
Before farmingbefore 6500 BC34%22 of 65 copies read
First farmers6500 to 3000 BC40%398 of 987 copies read
Bronze Age3000 to 1200 BC40%372 of 932 copies read
Iron Age and Antiquity1200 BC to AD 60040%452 of 1,139 copies read
Middle AgesAD 600 to 150046%296 of 643 copies read
Today1000 Genomes34%340 of 1,006 copies

Neanderthal and Denisovan genomes

Altai Neanderthal
2 copies
Vindija Neanderthal
2 copies
Chagyrskaya Neanderthal
2 copies
Denisovan
No copies
For most ancient people only one of their two copies can be read, so these counts are copies read, not people. Close relatives, repeated samples and samples the archive marks as unreliable are left out. Damage in old DNA can fake this letter, so it is counted only from samples treated to remove that damage and from high-quality genomes. Ancient genomes from the Allen Ancient DNA Resource (AADR v66): 15,136 people.
rs1268789

The marker

Gene or region
FRAS1
Marker
rs1268789
Location
Chromosome 4 · GRCh37 79,280,693 · GRCh38 78,359,539
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
FRAS1 · rs1268789
Location
Chromosome 4 · GRCh37 79,280,693 · GRCh38 78,359,539
Studied allele
T
Published statistic
Per T: 0.076 European discovery meta-analysis (P 4.9e-15); replication POL 0.102 (P 0.021), US 0.087 (P 0.014), CANDELA 0.025 (P 0.058), ERF 0.001 (P 0.99); non-Asian meta-analysis 0.051 (P 1.5e-14) (Supplementary Table 2); reported earlier by Medland 2009 at P 7e-8 (Supplementary Table 6); its r2 0.98 proxy rs506863 has OR 1.27 per C (Table 2) (Supplementary Table 2 (rs1268789 row, US column: frequency 0.317, beta 0.0865, SE 0.0350, P 0.014) and Methods (US three level curliness scale))
1000 Genomes Project phase 3, people with 0, 1 and 2 copies
All regions 811 / 1098 / 595 · Africa 310 / 293 / 58 · The Americas 152 / 154 / 41 · East Asia 31 / 197 / 276 · Europe 221 / 224 / 58 · South Asia 97 / 230 / 162
See this card in the sample report
Limits

What it cannot tell you

The same topic

More in Appearance

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