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rs398122882

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CC;CC) 0 common in clinvar
Make rs398122882(-;-)
Make rs398122882(-;CC)
ReferenceGRCh38 38.1/141
Chromosome2
Position120970411
GeneGLI2
is asnp
is mentioned by
dbSNPrs398122882
ebirs398122882
HLIrs398122882
Exacrs398122882
Varsomers398122882
Maprs398122882
PheGenIrs398122882
hapmaprs398122882
1000 genomesrs398122882
hgdprs398122882
ensemblrs398122882
gopubmedrs398122882
geneviewrs398122882
scholarrs398122882
googlers398122882
pharmgkbrs398122882
gwascentralrs398122882
openSNPrs398122882
23andMers398122882
23andMe allrs398122882
SNP Nexus

SNPshotrs398122882
SNPdbers398122882
MSV3drs398122882
GWAS Ctlgrs398122882
Max Magnitude0
ClinVar
Risk rs398122882(;)
Alt rs398122882(;)
Reference rs398122882(CC;CC)
Significance Pathogenic
Disease Holoprosencephaly 9
Variation info
Gene GLI2
CLNDBN Holoprosencephaly 9
Reversed 0
HGVS NC_000002.11:g.121727987_121727988delCC
CLNSRC OMIM Allelic Variant
CLNACC RCV000030729.23,