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rs876661327

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876661327(C;C)
Make rs876661327(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position120990675
GeneGLI2
is asnp
is mentioned by
dbSNPrs876661327
ebirs876661327
HLIrs876661327
Exacrs876661327
Varsomers876661327
Maprs876661327
PheGenIrs876661327
hapmaprs876661327
1000 genomesrs876661327
hgdprs876661327
ensemblrs876661327
gopubmedrs876661327
geneviewrs876661327
scholarrs876661327
googlers876661327
pharmgkbrs876661327
gwascentralrs876661327
openSNPrs876661327
23andMers876661327
23andMe allrs876661327
SNP Nexus

SNPshotrs876661327
SNPdbers876661327
MSV3drs876661327
GWAS Ctlgrs876661327
Max Magnitude0
ClinVar
Risk rs876661327(C;C)
Alt rs876661327(C;C)
Reference rs876661327(G;G)
Significance Probable-Pathogenic
Disease microform holoprosencephaly
Variation info
Gene GLI2
CLNDBN microform holoprosencephaly
Reversed 0
HGVS NC_000002.11:g.121748251G>C
CLNSRC
CLNACC RCV000223717.1,