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rs1064794983

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome17
Position41586482
GeneKRT14
is asnp
is mentioned by
dbSNPrs1064794983
dbSNP (old)rs1064794983
ClinGenrs1064794983
ebirs1064794983
HLIrs1064794983
Exacrs1064794983
Gnomadrs1064794983
Varsomers1064794983
Maprs1064794983
PheGenIrs1064794983
Biobankrs1064794983
1000 genomesrs1064794983
hgdprs1064794983
ensemblrs1064794983
gopubmedrs1064794983
geneviewrs1064794983
scholarrs1064794983
googlers1064794983
pharmgkbrs1064794983
gwascentralrs1064794983
openSNPrs1064794983
23andMers1064794983
23andMe allrs1064794983
SNPshotrs1064794983
SNPdbers1064794983
MSV3drs1064794983
GWAS Ctlgrs1064794983
Max Magnitude0
ClinVar
Risk rs1064794983(T;T)
Alt rs1064794983(T;T)
Reference Rs1064794983(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KRT14
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.39742734G>A
CLNSRC
CLNACC RCV000487128.1,