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rs104894961

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104894961(C;C)
Make rs104894961(C;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position137567449
GeneZIC3
is asnp
is mentioned by
dbSNPrs104894961
ebirs104894961
HLIrs104894961
Exacrs104894961
Varsomers104894961
Maprs104894961
PheGenIrs104894961
hapmaprs104894961
1000 genomesrs104894961
hgdprs104894961
ensemblrs104894961
gopubmedrs104894961
geneviewrs104894961
scholarrs104894961
googlers104894961
pharmgkbrs104894961
gwascentralrs104894961
openSNPrs104894961
23andMers104894961
23andMe allrs104894961
SNP Nexus

SNPshotrs104894961
SNPdbers104894961
MSV3drs104894961
GWAS Ctlgrs104894961
Max Magnitude0
OMIM300265
Desc
Variant0005
Relatedalso
ClinVar
Risk rs104894961(C;C)
Alt rs104894961(C;C)
Reference rs104894961(G;G)
Significance Pathogenic
Disease Heterotaxy
Variation info
Gene ZIC3
CLNDBN Heterotaxy, visceral, X-linked
Reversed 0
HGVS NC_000023.10:g.136649608G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000012190.2,