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rs387907171

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387907171(C;T)
Make rs387907171(T;T)
ReferenceGRCh37.p10 37.5/138
Chromosome9
Position12694273
GeneTYRP1
is asnp
is mentioned by
dbSNPrs387907171
ebirs387907171
HLIrs387907171
Exacrs387907171
Varsomers387907171
Maprs387907171
PheGenIrs387907171
hapmaprs387907171
1000 genomesrs387907171
hgdprs387907171
ensemblrs387907171
gopubmedrs387907171
geneviewrs387907171
scholarrs387907171
googlers387907171
pharmgkbrs387907171
gwascentralrs387907171
openSNPrs387907171
23andMers387907171
23andMe allrs387907171
SNP Nexus

SNPshotrs387907171
SNPdbers387907171
MSV3drs387907171
GWAS Ctlgrs387907171
Max Magnitude0
ClinVar
Risk rs387907171(T;T)
Alt rs387907171(T;T)
Reference rs387907171(C;C)
Significance Other
Disease Skin/hair/eye pigmentation
Variation info
Gene TYRP1
CLNDBN Skin/hair/eye pigmentation, variation in, 11
Reversed 0
HGVS NC_000009.11:g.12694273C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000024318.29,