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rs121917710

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121917710(A;A)
Make rs121917710(A;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position41967848
GeneGLI3
is asnp
is mentioned by
dbSNPrs121917710
ebirs121917710
HLIrs121917710
Exacrs121917710
Varsomers121917710
Maprs121917710
PheGenIrs121917710
hapmaprs121917710
1000 genomesrs121917710
hgdprs121917710
ensemblrs121917710
gopubmedrs121917710
geneviewrs121917710
scholarrs121917710
googlers121917710
pharmgkbrs121917710
gwascentralrs121917710
openSNPrs121917710
23andMers121917710
23andMe allrs121917710
SNP Nexus

SNPshotrs121917710
SNPdbers121917710
MSV3drs121917710
GWAS Ctlgrs121917710
GMAF0.002296
Max Magnitude0
OMIM165240
Desc
Variant0009
Relatedalso
ClinVar
Risk rs121917710(A;A)
Alt rs121917710(A;A)
Reference rs121917710(G;G)
Significance Pathogenic
Disease not provided not specified
Variation info
Gene GLI3
CLNDBN not provided not specified
Reversed 1
HGVS NC_000007.13:g.42007446C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000014832.21, RCV000174664.1,