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rs121909072

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121909072(A;A)
Make rs121909072(A;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position42606560
GeneTNFSF11
is asnp
is mentioned by
dbSNPrs121909072
ebirs121909072
HLIrs121909072
Exacrs121909072
Varsomers121909072
Maprs121909072
PheGenIrs121909072
hapmaprs121909072
1000 genomesrs121909072
hgdprs121909072
ensemblrs121909072
gopubmedrs121909072
geneviewrs121909072
scholarrs121909072
googlers121909072
pharmgkbrs121909072
gwascentralrs121909072
openSNPrs121909072
23andMers121909072
23andMe allrs121909072
SNP Nexus

SNPshotrs121909072
SNPdbers121909072
MSV3drs121909072
GWAS Ctlgrs121909072
Max Magnitude0
OMIM602642
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121909072(A;A)
Alt rs121909072(A;A)
Reference rs121909072(T;T)
Significance Pathogenic
Disease Osteopetrosis autosomal recessive 2
Variation info
Gene TNFSF11
CLNDBN Osteopetrosis autosomal recessive 2
Reversed 0
HGVS NC_000013.10:g.43180696T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000007389.3,