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rs794729641

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794729641(G;G)
Make rs794729641(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position99985328
GeneZIC2
is asnp
is mentioned by
dbSNPrs794729641
ebirs794729641
HLIrs794729641
Exacrs794729641
Varsomers794729641
Maprs794729641
PheGenIrs794729641
hapmaprs794729641
1000 genomesrs794729641
hgdprs794729641
ensemblrs794729641
gopubmedrs794729641
geneviewrs794729641
scholarrs794729641
googlers794729641
pharmgkbrs794729641
gwascentralrs794729641
openSNPrs794729641
23andMers794729641
23andMe allrs794729641
SNP Nexus

SNPshotrs794729641
SNPdbers794729641
MSV3drs794729641
GWAS Ctlgrs794729641
Max Magnitude0
ClinVar
Risk rs794729641(G;G)
Alt rs794729641(G;G)
Reference rs794729641(T;T)
Significance Probable-Pathogenic
Disease Holoprosencephaly 5
Variation info
Gene ZIC2
CLNDBN Holoprosencephaly 5
Reversed 0
HGVS NC_000013.10:g.100637582T>G
CLNSRC
CLNACC RCV000185543.2,