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rs4959270

From SNPedia

Orientationplus
Stabilizedplus
Make rs4959270(A;A)
Make rs4959270(A;C)
Make rs4959270(C;C)
ReferenceGRCh37.p5 37.3/135
Chromosome6
Position457748
GeneLOC105374875
is asnp
is mentioned by
dbSNPrs4959270
dbSNP (classic)rs4959270
ClinGenrs4959270
ebirs4959270
HLIrs4959270
Exacrs4959270
Gnomadrs4959270
Varsomers4959270
LitVarrs4959270
Maprs4959270
PheGenIrs4959270
Biobankrs4959270
1000 genomesrs4959270
hgdprs4959270
ensemblrs4959270
geneviewrs4959270
scholarrs4959270
googlers4959270
pharmgkbrs4959270
gwascentralrs4959270
openSNPrs4959270
23andMers4959270
SNPshotrs4959270
SNPdbers4959270
MSV3drs4959270
GWAS Ctlgrs4959270
GMAF0.3737
Max Magnitude0
? (A;A) (A;C) (C;C) 28


[PMID 21197618OA-icon.png] Model-based prediction of human hair color using DNA variants [1] EXOC2 (rs4959270 allelic OR for A vs. C: 0.56; 95% CI: [0.35–0.91]; P = 0.02) were most significantly associated with black hair color .


[PMID 17952075] Genetic determinants of hair, eye and skin pigmentation in Europeans.[2]


[PMID 18483556OA-icon.png] A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation.


[PMID 19340012OA-icon.png] Genome-wide association study of tanning phenotype in a population of European ancestry.


[PMID 20383147OA-icon.png] Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus.