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rs1064794694

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
ChromosomeX
Position53432035
GeneHSD17B10
is asnp
is mentioned by
dbSNPrs1064794694
dbSNP (old)rs1064794694
ClinGenrs1064794694
ebirs1064794694
HLIrs1064794694
Exacrs1064794694
Gnomadrs1064794694
Varsomers1064794694
LitVarrs1064794694
Maprs1064794694
PheGenIrs1064794694
Biobankrs1064794694
1000 genomesrs1064794694
hgdprs1064794694
ensemblrs1064794694
gopubmedrs1064794694
geneviewrs1064794694
scholarrs1064794694
googlers1064794694
pharmgkbrs1064794694
gwascentralrs1064794694
openSNPrs1064794694
23andMers1064794694
23andMe allrs1064794694
SNPshotrs1064794694
SNPdbers1064794694
MSV3drs1064794694
GWAS Ctlgrs1064794694
Max Magnitude0
ClinVar
Risk rs1064794694(T;T)
Alt rs1064794694(T;T)
Reference Rs1064794694(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene HSD17B10
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.53458983G>A
CLNSRC
CLNACC RCV000484484.1,