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rs876661325

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876661325(-;-)
Make rs876661325(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position120986385
GeneGLI2
is asnp
is mentioned by
dbSNPrs876661325
ebirs876661325
HLIrs876661325
Exacrs876661325
Varsomers876661325
Maprs876661325
PheGenIrs876661325
hapmaprs876661325
1000 genomesrs876661325
hgdprs876661325
ensemblrs876661325
gopubmedrs876661325
geneviewrs876661325
scholarrs876661325
googlers876661325
pharmgkbrs876661325
gwascentralrs876661325
openSNPrs876661325
23andMers876661325
23andMe allrs876661325
SNP Nexus

SNPshotrs876661325
SNPdbers876661325
MSV3drs876661325
GWAS Ctlgrs876661325
Max Magnitude0
ClinVar
Risk rs876661325(;)
Alt rs876661325(;)
Reference rs876661325(C;C)
Significance Probable-Pathogenic
Disease microform holoprosencephaly
Variation info
Gene GLI2
CLNDBN microform holoprosencephaly
Reversed 0
HGVS NC_000002.11:g.121743961delC
CLNSRC
CLNACC RCV000223797.1,