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rs113369052

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs113369052(A;A)
Make rs113369052(A;T)
ReferenceGRCh38 38.1/142
Chromosome12
Position52487957
GeneKRT6A
is asnp
is mentioned by
dbSNPrs113369052
ebirs113369052
HLIrs113369052
Exacrs113369052
Varsomers113369052
Maprs113369052
PheGenIrs113369052
hapmaprs113369052
1000 genomesrs113369052
hgdprs113369052
ensemblrs113369052
gopubmedrs113369052
geneviewrs113369052
scholarrs113369052
googlers113369052
pharmgkbrs113369052
gwascentralrs113369052
openSNPrs113369052
23andMers113369052
23andMe allrs113369052
SNP Nexus

SNPshotrs113369052
SNPdbers113369052
MSV3drs113369052
GWAS Ctlgrs113369052
Max Magnitude0
ClinVar
Risk rs113369052(A,G;A,G)
Alt rs113369052(A,G;A,G)
Reference rs113369052(T;T)
Significance Pathogenic
Disease PC-K6a
Variation info
Gene KRT6A
CLNDBN PC-K6a
Reversed 0
HGVS NC_000012.11:g.52881741T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000144079.2,