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rs398122938

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398122938(C;C)
Make rs398122938(C;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position64921855
GeneZC4H2
is asnp
is mentioned by
dbSNPrs398122938
ebirs398122938
HLIrs398122938
Exacrs398122938
Varsomers398122938
Maprs398122938
PheGenIrs398122938
hapmaprs398122938
1000 genomesrs398122938
hgdprs398122938
ensemblrs398122938
gopubmedrs398122938
geneviewrs398122938
scholarrs398122938
googlers398122938
pharmgkbrs398122938
gwascentralrs398122938
openSNPrs398122938
23andMers398122938
23andMe allrs398122938
SNP Nexus

SNPshotrs398122938
SNPdbers398122938
MSV3drs398122938
GWAS Ctlgrs398122938
Max Magnitude0
ClinVar
Risk rs398122938(C;C)
Alt rs398122938(C;C)
Reference rs398122938(G;G)
Significance Pathogenic
Disease Wieacker syndrome
Variation info
Gene ZC4H2
CLNDBN Wieacker syndrome
Reversed 1
HGVS NC_000023.10:g.64141735C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000043676.4,