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rs879255236

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs879255236(C;T)
Make rs879255236(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position64917821
GeneZC4H2
is asnp
is mentioned by
dbSNPrs879255236
ebirs879255236
HLIrs879255236
Exacrs879255236
Varsomers879255236
Maprs879255236
PheGenIrs879255236
hapmaprs879255236
1000 genomesrs879255236
hgdprs879255236
ensemblrs879255236
gopubmedrs879255236
geneviewrs879255236
scholarrs879255236
googlers879255236
pharmgkbrs879255236
gwascentralrs879255236
openSNPrs879255236
23andMers879255236
23andMe allrs879255236
SNP Nexus

SNPshotrs879255236
SNPdbers879255236
MSV3drs879255236
GWAS Ctlgrs879255236
Max Magnitude0
ClinVar
Risk rs879255236(T;T)
Alt rs879255236(T;T)
Reference rs879255236(C;C)
Significance Pathogenic
Disease Wieacker syndrome
Variation info
Gene ZC4H2
CLNDBN Wieacker syndrome
Reversed 1
HGVS NC_000023.10:g.64137701G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000043679.3,