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rs61157095

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs61157095(C;C)
Make rs61157095(C;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position41571490
GeneKRT9
is asnp
is mentioned by
dbSNPrs61157095
ebirs61157095
HLIrs61157095
Exacrs61157095
Varsomers61157095
Maprs61157095
PheGenIrs61157095
hapmaprs61157095
1000 genomesrs61157095
hgdprs61157095
ensemblrs61157095
gopubmedrs61157095
geneviewrs61157095
scholarrs61157095
googlers61157095
pharmgkbrs61157095
gwascentralrs61157095
openSNPrs61157095
23andMers61157095
23andMe allrs61157095
SNP Nexus

SNPshotrs61157095
SNPdbers61157095
MSV3drs61157095
GWAS Ctlgrs61157095
Max Magnitude0
OMIM607606
Desc
Variant0008
Relatedalso


ClinVar
Risk rs61157095(C;C)
Alt rs61157095(C;C)
Reference rs61157095(T;T)
Significance Pathogenic
Disease Epidermolytic palmoplantar keratoderma not provided
Variation info
Gene KRT9
CLNDBN Epidermolytic palmoplantar keratoderma not provided
Reversed 1
HGVS NC_000017.10:g.39727742A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000003140.2, RCV000056469.1,