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rs397515500

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs397515500(-;-)
Make rs397515500(-;AG)
ReferenceGRCh38 38.1/141
Chromosome13
Position99984961
GeneZIC2
is asnp
is mentioned by
dbSNPrs397515500
ebirs397515500
HLIrs397515500
Exacrs397515500
Varsomers397515500
Maprs397515500
PheGenIrs397515500
hapmaprs397515500
1000 genomesrs397515500
hgdprs397515500
ensemblrs397515500
gopubmedrs397515500
geneviewrs397515500
scholarrs397515500
googlers397515500
pharmgkbrs397515500
gwascentralrs397515500
openSNPrs397515500
23andMers397515500
23andMe allrs397515500
SNP Nexus

SNPshotrs397515500
SNPdbers397515500
MSV3drs397515500
GWAS Ctlgrs397515500
Max Magnitude0
ClinVar
Risk rs397515500(;)
Alt rs397515500(;)
Reference rs397515500(AG;AG)
Significance Pathogenic
Disease Holoprosencephaly 5
Variation info
Gene ZIC2
CLNDBN Holoprosencephaly 5
Reversed 0
HGVS NC_000013.10:g.100637215_100637216delAG
CLNSRC ClinVar GeneReviews
CLNACC RCV000055679.1,