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rs1064795680

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
ChromosomeX
Position64921842
GeneZC4H2
is asnp
is mentioned by
dbSNPrs1064795680
dbSNP (old)rs1064795680
ClinGenrs1064795680
ebirs1064795680
HLIrs1064795680
Exacrs1064795680
Gnomadrs1064795680
Varsomers1064795680
Maprs1064795680
PheGenIrs1064795680
Biobankrs1064795680
1000 genomesrs1064795680
hgdprs1064795680
ensemblrs1064795680
gopubmedrs1064795680
geneviewrs1064795680
scholarrs1064795680
googlers1064795680
pharmgkbrs1064795680
gwascentralrs1064795680
openSNPrs1064795680
23andMers1064795680
23andMe allrs1064795680
SNPshotrs1064795680
SNPdbers1064795680
MSV3drs1064795680
GWAS Ctlgrs1064795680
Max Magnitude0
ClinVar
Risk rs1064795680(A;A)
Alt rs1064795680(A;A)
Reference Rs1064795680(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ZC4H2
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.64141722C>T
CLNSRC
CLNACC RCV000478352.1,