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rs397515364

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397515364(-;-)
Make rs397515364(-;C)
Make rs397515364(C;C)
ReferenceGRCh38 38.1/141
Chromosome13
Position99985401
GeneZIC2
is asnp
is mentioned by
dbSNPrs397515364
ebirs397515364
HLIrs397515364
Exacrs397515364
Varsomers397515364
Maprs397515364
PheGenIrs397515364
hapmaprs397515364
1000 genomesrs397515364
hgdprs397515364
ensemblrs397515364
gopubmedrs397515364
geneviewrs397515364
scholarrs397515364
googlers397515364
pharmgkbrs397515364
gwascentralrs397515364
openSNPrs397515364
23andMers397515364
23andMe allrs397515364
SNP Nexus

SNPshotrs397515364
SNPdbers397515364
MSV3drs397515364
GWAS Ctlgrs397515364
Max Magnitude0
ClinVar
Risk rs397515364(C;C)
Alt rs397515364(C;C)
Reference rs397515364(;)
Significance Pathogenic
Disease Holoprosencephaly 5
Variation info
Gene ZIC2
CLNDBN Holoprosencephaly 5
Reversed 0
HGVS NC_000013.10:g.100637655dupC
CLNSRC OMIM Allelic Variant
CLNACC RCV000007017.2,