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rs879255362

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs879255362(G;T)
Make rs879255362(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position64917850
GeneZC4H2
is asnp
is mentioned by
dbSNPrs879255362
ebirs879255362
HLIrs879255362
Exacrs879255362
Varsomers879255362
Maprs879255362
PheGenIrs879255362
hapmaprs879255362
1000 genomesrs879255362
hgdprs879255362
ensemblrs879255362
gopubmedrs879255362
geneviewrs879255362
scholarrs879255362
googlers879255362
pharmgkbrs879255362
gwascentralrs879255362
openSNPrs879255362
23andMers879255362
23andMe allrs879255362
SNP Nexus

SNPshotrs879255362
SNPdbers879255362
MSV3drs879255362
GWAS Ctlgrs879255362
Max Magnitude0
ClinVar
Risk rs879255362(T;T)
Alt rs879255362(T;T)
Reference rs879255362(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ZC4H2
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.64137730C>A
CLNSRC
CLNACC RCV000238874.1,