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rs876661324

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876661324(C;T)
Make rs876661324(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position120968860
GeneGLI2
is asnp
is mentioned by
dbSNPrs876661324
ebirs876661324
HLIrs876661324
Exacrs876661324
Varsomers876661324
Maprs876661324
PheGenIrs876661324
hapmaprs876661324
1000 genomesrs876661324
hgdprs876661324
ensemblrs876661324
gopubmedrs876661324
geneviewrs876661324
scholarrs876661324
googlers876661324
pharmgkbrs876661324
gwascentralrs876661324
openSNPrs876661324
23andMers876661324
23andMe allrs876661324
SNP Nexus

SNPshotrs876661324
SNPdbers876661324
MSV3drs876661324
GWAS Ctlgrs876661324
Max Magnitude0
ClinVar
Risk rs876661324(T;T)
Alt rs876661324(T;T)
Reference rs876661324(C;C)
Significance Probable-Pathogenic
Disease microform holoprosencephaly
Variation info
Gene GLI2
CLNDBN microform holoprosencephaly
Reversed 0
HGVS NC_000002.11:g.121726436C>T
CLNSRC
CLNACC RCV000223706.1,