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rs104894960

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104894960(C;T)
Make rs104894960(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position137567436
GeneZIC3
is asnp
is mentioned by
dbSNPrs104894960
ebirs104894960
HLIrs104894960
Exacrs104894960
Varsomers104894960
Maprs104894960
PheGenIrs104894960
hapmaprs104894960
1000 genomesrs104894960
hgdprs104894960
ensemblrs104894960
gopubmedrs104894960
geneviewrs104894960
scholarrs104894960
googlers104894960
pharmgkbrs104894960
gwascentralrs104894960
openSNPrs104894960
23andMers104894960
23andMe allrs104894960
SNP Nexus

SNPshotrs104894960
SNPdbers104894960
MSV3drs104894960
GWAS Ctlgrs104894960
Max Magnitude0
OMIM300265
Desc
Variant0004
Relatedalso
ClinVar
Risk rs104894960(T;T)
Alt rs104894960(T;T)
Reference rs104894960(C;C)
Significance Pathogenic
Disease Heterotaxy
Variation info
Gene ZIC3
CLNDBN Heterotaxy, visceral, X-linked
Reversed 0
HGVS NC_000023.10:g.136649595C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000012189.11,