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rs876661326

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876661326(A;A)
Make rs876661326(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position120986558
GeneGLI2
is asnp
is mentioned by
dbSNPrs876661326
ebirs876661326
HLIrs876661326
Exacrs876661326
Varsomers876661326
Maprs876661326
PheGenIrs876661326
hapmaprs876661326
1000 genomesrs876661326
hgdprs876661326
ensemblrs876661326
gopubmedrs876661326
geneviewrs876661326
scholarrs876661326
googlers876661326
pharmgkbrs876661326
gwascentralrs876661326
openSNPrs876661326
23andMers876661326
23andMe allrs876661326
SNP Nexus

SNPshotrs876661326
SNPdbers876661326
MSV3drs876661326
GWAS Ctlgrs876661326
Max Magnitude0
ClinVar
Risk rs876661326(A;A)
Alt rs876661326(A;A)
Reference rs876661326(G;G)
Significance Probable-Pathogenic
Disease microform holoprosencephaly
Variation info
Gene GLI2
CLNDBN microform holoprosencephaly
Reversed 0
HGVS NC_000002.11:g.121744134G>A
CLNSRC
CLNACC RCV000223883.1,