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rs1064793977

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome12
Position52520296
GeneKRT5
is asnp
is mentioned by
dbSNPrs1064793977
dbSNP (old)rs1064793977
ClinGenrs1064793977
ebirs1064793977
HLIrs1064793977
Exacrs1064793977
Gnomadrs1064793977
Varsomers1064793977
Maprs1064793977
PheGenIrs1064793977
Biobankrs1064793977
1000 genomesrs1064793977
hgdprs1064793977
ensemblrs1064793977
gopubmedrs1064793977
geneviewrs1064793977
scholarrs1064793977
googlers1064793977
pharmgkbrs1064793977
gwascentralrs1064793977
openSNPrs1064793977
23andMers1064793977
23andMe allrs1064793977
SNPshotrs1064793977
SNPdbers1064793977
MSV3drs1064793977
GWAS Ctlgrs1064793977
Max Magnitude0
ClinVar
Risk rs1064793977(G;G)
Alt rs1064793977(G;G)
Reference Rs1064793977(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene KRT5
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.52914080T>C
CLNSRC
CLNACC RCV000484793.1,