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rs797044863

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs797044863(C;T)
Make rs797044863(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position64921894
GeneZC4H2
is asnp
is mentioned by
dbSNPrs797044863
ebirs797044863
HLIrs797044863
Exacrs797044863
Varsomers797044863
Maprs797044863
PheGenIrs797044863
hapmaprs797044863
1000 genomesrs797044863
hgdprs797044863
ensemblrs797044863
gopubmedrs797044863
geneviewrs797044863
scholarrs797044863
googlers797044863
pharmgkbrs797044863
gwascentralrs797044863
openSNPrs797044863
23andMers797044863
23andMe allrs797044863
SNP Nexus

SNPshotrs797044863
SNPdbers797044863
MSV3drs797044863
GWAS Ctlgrs797044863
Max Magnitude0
ClinVar
Risk rs797044863(T;T)
Alt rs797044863(T;T)
Reference rs797044863(C;C)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene ZC4H2
CLNDBN Inborn genetic diseases
Reversed 1
HGVS NC_000023.10:g.64141774G>A
CLNSRC
CLNACC RCV000190667.1,