Have questions? Visit https://www.reddit.com/r/SNPedia

rs397515499

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397515499(-;-)
Make rs397515499(-;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position99983000
GeneZIC2
is asnp
is mentioned by
dbSNPrs397515499
ebirs397515499
HLIrs397515499
Exacrs397515499
Varsomers397515499
Maprs397515499
PheGenIrs397515499
hapmaprs397515499
1000 genomesrs397515499
hgdprs397515499
ensemblrs397515499
gopubmedrs397515499
geneviewrs397515499
scholarrs397515499
googlers397515499
pharmgkbrs397515499
gwascentralrs397515499
openSNPrs397515499
23andMers397515499
23andMe allrs397515499
SNP Nexus

SNPshotrs397515499
SNPdbers397515499
MSV3drs397515499
GWAS Ctlgrs397515499
Max Magnitude0
ClinVar
Risk rs397515499(;)
Alt rs397515499(;)
Reference rs397515499(G;G)
Significance Pathogenic
Disease Holoprosencephaly 5
Variation info
Gene ZIC2
CLNDBN Holoprosencephaly 5
Reversed 0
HGVS NC_000013.10:g.100635254delG
CLNSRC ClinVar GeneReviews
CLNACC RCV000055674.1,