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rs61145796

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs61145796(C;C)
Make rs61145796(C;T)
ReferenceGRCh38 38.1/142
Chromosome12
Position52492668
GeneKRT6A
is asnp
is mentioned by
dbSNPrs61145796
ebirs61145796
HLIrs61145796
Exacrs61145796
Varsomers61145796
Maprs61145796
PheGenIrs61145796
hapmaprs61145796
1000 genomesrs61145796
hgdprs61145796
ensemblrs61145796
gopubmedrs61145796
geneviewrs61145796
scholarrs61145796
googlers61145796
pharmgkbrs61145796
gwascentralrs61145796
openSNPrs61145796
23andMers61145796
23andMe allrs61145796
SNP Nexus

SNPshotrs61145796
SNPdbers61145796
MSV3drs61145796
GWAS Ctlgrs61145796
Max Magnitude0


ClinVar
Risk rs61145796(C,G;C,G)
Alt rs61145796(C,G;C,G)
Reference rs61145796(T;T)
Significance Pathogenic
Disease not provided PC-K6a
Variation info
Gene KRT6A
CLNDBN not provided PC-K6a
Reversed 1
HGVS NC_000012.11:g.52886452A>C; NC_000012.11:g.52886452A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000057015.1, RCV000057014.1, RCV000144078.2,