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rs122463167

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs122463167(A;A)
Make rs122463167(A;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position137567448
GeneZIC3
is asnp
is mentioned by
dbSNPrs122463167
dbSNP (classic)rs122463167
ClinGenrs122463167
ebirs122463167
HLIrs122463167
Exacrs122463167
Gnomadrs122463167
Varsomers122463167
LitVarrs122463167
Maprs122463167
PheGenIrs122463167
Biobankrs122463167
1000 genomesrs122463167
hgdprs122463167
ensemblrs122463167
geneviewrs122463167
scholarrs122463167
googlers122463167
pharmgkbrs122463167
gwascentralrs122463167
openSNPrs122463167
23andMers122463167
SNPshotrs122463167
SNPdbers122463167
MSV3drs122463167
GWAS Ctlgrs122463167
Max Magnitude0
OMIM300265
Desc
Variant0005
Relatedalso
ClinVar
Risk rs122463167(A;A)
Alt rs122463167(A;A)
Reference Rs122463167(T;T)
Significance Untested
Disease Heterotaxy
Variation info
Gene ZIC3
CLNDBN Heterotaxy, visceral, X-linked
Reversed 0
HGVS NC_000023.10:g.136649607T>A
CLNSRC OMIM Allelic Variant
CLNACC SCV000032424.1, SCV000032424.1,