This variant maps to 2 locations
Alleles
C/T|Ancestral: C|MAF: 0.38 (T)
Location
This variant maps to 2 genomic locations; None selected
Evidence status 
Clinical significance
HGVS name
NM_004667.5:c.323-4749G>A
Synonyms
This variant has 3 synonyms - Show
Genotyping chips
This variant has assays on 12 chips - Show
Original source
Variants (including SNPs and indels) imported from dbSNP (release 149)|View in dbSNP
About this variant
This variant has 3952 sample genotypes, is associated with 12 phenotypes and is mentioned in 16 citations.
Description from SNPedia
rs1667394 increases susceptibility to Blond rather than brown hair 4.94 times for carriers of the A allele [PMID:17952075]... Show
