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rs387906498

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs387906498(A;T)
Make rs387906498(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position137569063
GeneZIC3
is asnp
is mentioned by
dbSNPrs387906498
ebirs387906498
HLIrs387906498
Exacrs387906498
Varsomers387906498
Maprs387906498
PheGenIrs387906498
hapmaprs387906498
1000 genomesrs387906498
hgdprs387906498
ensemblrs387906498
gopubmedrs387906498
geneviewrs387906498
scholarrs387906498
googlers387906498
pharmgkbrs387906498
gwascentralrs387906498
openSNPrs387906498
23andMers387906498
23andMe allrs387906498
SNP Nexus

SNPshotrs387906498
SNPdbers387906498
MSV3drs387906498
GWAS Ctlgrs387906498
Max Magnitude0
ClinVar
Risk rs387906498(T;T)
Alt rs387906498(T;T)
Reference rs387906498(A;A)
Significance Pathogenic
Disease Congenital heart defects
Variation info
Gene ZIC3
CLNDBN Congenital heart defects, multiple types, 1, X-linked
Reversed 0
HGVS NC_000023.10:g.136651222A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000012188.11,