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rs28933372

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0
(G;G) 0 common in clinvar
Make rs28933372(C;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position41966273
GeneGLI3
is asnp
is mentioned by
dbSNPrs28933372
ebirs28933372
HLIrs28933372
Exacrs28933372
Varsomers28933372
Maprs28933372
PheGenIrs28933372
hapmaprs28933372
1000 genomesrs28933372
hgdprs28933372
ensemblrs28933372
gopubmedrs28933372
geneviewrs28933372
scholarrs28933372
googlers28933372
pharmgkbrs28933372
gwascentralrs28933372
openSNPrs28933372
23andMers28933372
23andMe allrs28933372
SNP Nexus

SNPshotrs28933372
SNPdbers28933372
MSV3drs28933372
GWAS Ctlgrs28933372
Max Magnitude0
OMIM165240
DescACROCALLOSAL SYNDROME
Variant0013
Relatedalso


ClinVar
Risk rs28933372(C;C)
Alt rs28933372(C;C)
Reference rs28933372(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene GLI3
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.42005871C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000030896.25,