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rs876661323

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876661323(-;-)
Make rs876661323(-;G)
Make rs876661323(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position120955383
GeneGLI2
is asnp
is mentioned by
dbSNPrs876661323
ebirs876661323
HLIrs876661323
Exacrs876661323
Varsomers876661323
Maprs876661323
PheGenIrs876661323
hapmaprs876661323
1000 genomesrs876661323
hgdprs876661323
ensemblrs876661323
gopubmedrs876661323
geneviewrs876661323
scholarrs876661323
googlers876661323
pharmgkbrs876661323
gwascentralrs876661323
openSNPrs876661323
23andMers876661323
23andMe allrs876661323
SNP Nexus

SNPshotrs876661323
SNPdbers876661323
MSV3drs876661323
GWAS Ctlgrs876661323
Max Magnitude0
ClinVar
Risk rs876661323(G;G)
Alt rs876661323(G;G)
Reference rs876661323(;)
Significance Probable-Pathogenic
Disease microform holoprosencephaly
Variation info
Gene GLI2
CLNDBN microform holoprosencephaly
Reversed 0
HGVS NC_000002.11:g.121712959dupG
CLNSRC
CLNACC RCV000223840.1,