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rs104894962

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs104894962(A;G)
Make rs104894962(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position137569054
GeneZIC3
is asnp
is mentioned by
dbSNPrs104894962
ebirs104894962
HLIrs104894962
Exacrs104894962
Varsomers104894962
Maprs104894962
PheGenIrs104894962
hapmaprs104894962
1000 genomesrs104894962
hgdprs104894962
ensemblrs104894962
gopubmedrs104894962
geneviewrs104894962
scholarrs104894962
googlers104894962
pharmgkbrs104894962
gwascentralrs104894962
openSNPrs104894962
23andMers104894962
23andMe allrs104894962
SNP Nexus

SNPshotrs104894962
SNPdbers104894962
MSV3drs104894962
GWAS Ctlgrs104894962
Max Magnitude0
OMIM300265
Desc
Variant0006
Relatedalso
ClinVar
Risk rs104894962(G;G)
Alt rs104894962(G;G)
Reference rs104894962(A;A)
Significance Pathogenic
Disease Heterotaxy
Variation info
Gene ZIC3
CLNDBN Heterotaxy, visceral, X-linked
Reversed 0
HGVS NC_000023.10:g.136651213A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000012191.20,