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rs104894963

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104894963(C;G)
Make rs104894963(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position137567340
GeneZIC3
is asnp
is mentioned by
dbSNPrs104894963
ebirs104894963
HLIrs104894963
Exacrs104894963
Varsomers104894963
Maprs104894963
PheGenIrs104894963
hapmaprs104894963
1000 genomesrs104894963
hgdprs104894963
ensemblrs104894963
gopubmedrs104894963
geneviewrs104894963
scholarrs104894963
googlers104894963
pharmgkbrs104894963
gwascentralrs104894963
openSNPrs104894963
23andMers104894963
23andMe allrs104894963
SNP Nexus

SNPshotrs104894963
SNPdbers104894963
MSV3drs104894963
GWAS Ctlgrs104894963
GMAF0.003023
Max Magnitude0
OMIM300265
Desc
Variant0007
Relatedalso
ClinVar
Risk rs104894963(G;G)
Alt rs104894963(G;G)
Reference rs104894963(C;C)
Significance Pathogenic
Disease Congenital heart defects not specified
Variation info
Gene ZIC3
CLNDBN Congenital heart defects, multiple types, 1, X-linked not specified
Reversed 0
HGVS NC_000023.10:g.136649499C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000012192.11, RCV000126382.2,