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rs1064795317

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome12
Position52651577
GeneKRT2
is asnp
is mentioned by
dbSNPrs1064795317
dbSNP (old)rs1064795317
ClinGenrs1064795317
ebirs1064795317
HLIrs1064795317
Exacrs1064795317
Gnomadrs1064795317
Varsomers1064795317
Maprs1064795317
PheGenIrs1064795317
Biobankrs1064795317
1000 genomesrs1064795317
hgdprs1064795317
ensemblrs1064795317
gopubmedrs1064795317
geneviewrs1064795317
scholarrs1064795317
googlers1064795317
pharmgkbrs1064795317
gwascentralrs1064795317
openSNPrs1064795317
23andMers1064795317
23andMe allrs1064795317
SNPshotrs1064795317
SNPdbers1064795317
MSV3drs1064795317
GWAS Ctlgrs1064795317
Max Magnitude0
ClinVar
Risk rs1064795317(C;C)
Alt rs1064795317(C;C)
Reference Rs1064795317(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KRT2
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.53045361A>G
CLNSRC
CLNACC RCV000483744.1,