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rs869312965

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312965(-;-)
Make rs869312965(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position120955349
GeneGLI2
is asnp
is mentioned by
dbSNPrs869312965
ebirs869312965
HLIrs869312965
Exacrs869312965
Varsomers869312965
Maprs869312965
PheGenIrs869312965
hapmaprs869312965
1000 genomesrs869312965
hgdprs869312965
ensemblrs869312965
gopubmedrs869312965
geneviewrs869312965
scholarrs869312965
googlers869312965
pharmgkbrs869312965
gwascentralrs869312965
openSNPrs869312965
23andMers869312965
23andMe allrs869312965
SNP Nexus

SNPshotrs869312965
SNPdbers869312965
MSV3drs869312965
GWAS Ctlgrs869312965
Max Magnitude0
ClinVar
Risk rs869312965(;)
Alt rs869312965(;)
Reference rs869312965(G;G)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene GLI2
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000002.11:g.121712925delG
CLNSRC
CLNACC RCV000210692.1,