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rs1064795753

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
ChromosomeX
Position64917841
GeneZC4H2
is asnp
is mentioned by
dbSNPrs1064795753
dbSNP (old)rs1064795753
ClinGenrs1064795753
ebirs1064795753
HLIrs1064795753
Exacrs1064795753
Gnomadrs1064795753
Varsomers1064795753
Maprs1064795753
PheGenIrs1064795753
Biobankrs1064795753
1000 genomesrs1064795753
hgdprs1064795753
ensemblrs1064795753
gopubmedrs1064795753
geneviewrs1064795753
scholarrs1064795753
googlers1064795753
pharmgkbrs1064795753
gwascentralrs1064795753
openSNPrs1064795753
23andMers1064795753
23andMe allrs1064795753
SNPshotrs1064795753
SNPdbers1064795753
MSV3drs1064795753
GWAS Ctlgrs1064795753
Max Magnitude0
ClinVar
Risk rs1064795753(T;T)
Alt rs1064795753(T;T)
Reference Rs1064795753(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ZC4H2
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.64137721C>A
CLNSRC
CLNACC RCV000484141.1,