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rs763608512

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs763608512(A;A)
Make rs763608512(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position52519825
GeneKRT5
is asnp
is mentioned by
dbSNPrs763608512
dbSNP (classic)rs763608512
ClinGenrs763608512
ebirs763608512
HLIrs763608512
Exacrs763608512
Gnomadrs763608512
Varsomers763608512
LitVarrs763608512
Maprs763608512
PheGenIrs763608512
Biobankrs763608512
1000 genomesrs763608512
hgdprs763608512
ensemblrs763608512
geneviewrs763608512
scholarrs763608512
googlers763608512
pharmgkbrs763608512
gwascentralrs763608512
openSNPrs763608512
23andMers763608512
23andMe allrs763608512
SNPshotrs763608512
SNPdbers763608512
MSV3drs763608512
GWAS Ctlgrs763608512
Max Magnitude0
ClinVar
Risk rs763608512(A;A) rs763608512(T;T)
Alt rs763608512(A;A) rs763608512(T;T)
Reference Rs763608512(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene KRT5
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.52913609C>A
CLNSRC
CLNACC RCV000435783.1,