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rs121912477

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121912477(A;G)
Make rs121912477(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position41612321
GeneKRT16
is asnp
is mentioned by
dbSNPrs121912477
ebirs121912477
HLIrs121912477
Exacrs121912477
Varsomers121912477
Maprs121912477
PheGenIrs121912477
hapmaprs121912477
1000 genomesrs121912477
hgdprs121912477
ensemblrs121912477
gopubmedrs121912477
geneviewrs121912477
scholarrs121912477
googlers121912477
pharmgkbrs121912477
gwascentralrs121912477
openSNPrs121912477
23andMers121912477
23andMe allrs121912477
SNP Nexus

SNPshotrs121912477
SNPdbers121912477
MSV3drs121912477
GWAS Ctlgrs121912477
Max Magnitude0
OMIM148067
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121912477(G;G)
Alt rs121912477(G;G)
Reference rs121912477(A;A)
Significance Pathogenic
Disease Palmoplantar keratoderma not provided
Variation info
Gene KRT16
CLNDBN Palmoplantar keratoderma, nonepidermolytic, focal not provided
Reversed 1
HGVS NC_000017.10:g.39768573T>C
CLNSRC Epithelial Biology OMIM Allelic Variant
CLNACC RCV000015706.24, RCV000057037.1,