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rs121909129

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909129(A;A)
Make rs121909129(A;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position52306270
GeneKRT86
is asnp
is mentioned by
dbSNPrs121909129
ebirs121909129
HLIrs121909129
Exacrs121909129
Varsomers121909129
Maprs121909129
PheGenIrs121909129
hapmaprs121909129
1000 genomesrs121909129
hgdprs121909129
ensemblrs121909129
gopubmedrs121909129
geneviewrs121909129
scholarrs121909129
googlers121909129
pharmgkbrs121909129
gwascentralrs121909129
openSNPrs121909129
23andMers121909129
23andMe allrs121909129
SNP Nexus

SNPshotrs121909129
SNPdbers121909129
MSV3drs121909129
GWAS Ctlgrs121909129
Max Magnitude0
OMIM601928
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121909129(A;A)
Alt rs121909129(A;A)
Reference rs121909129(G;G)
Significance Pathogenic
Disease Beaded hair not provided
Variation info
Gene KRT86
CLNDBN Beaded hair not provided
Reversed 0
HGVS NC_000012.11:g.52700054G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000008048.2, RCV000056959.1,