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rs398122899

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GA;GA) 0 common in clinvar
Make rs398122899(-;-)
Make rs398122899(-;GA)
ReferenceGRCh38 38.1/141
Chromosome7
Position41978629
GeneGLI3
is asnp
is mentioned by
dbSNPrs398122899
ebirs398122899
HLIrs398122899
Exacrs398122899
Varsomers398122899
Maprs398122899
PheGenIrs398122899
hapmaprs398122899
1000 genomesrs398122899
hgdprs398122899
ensemblrs398122899
gopubmedrs398122899
geneviewrs398122899
scholarrs398122899
googlers398122899
pharmgkbrs398122899
gwascentralrs398122899
openSNPrs398122899
23andMers398122899
23andMe allrs398122899
SNP Nexus

SNPshotrs398122899
SNPdbers398122899
MSV3drs398122899
GWAS Ctlgrs398122899
Max Magnitude0
ClinVar
Risk rs398122899(;)
Alt rs398122899(;)
Reference rs398122899(GA;GA)
Significance Pathogenic
Disease not provided
Variation info
Gene GLI3
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.42018228_42018229delTC
CLNSRC OMIM Allelic Variant
CLNACC RCV000032707.25,