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rs121908657

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908657(C;T)
Make rs121908657(T;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position62354492
GeneTNFRSF11A
is asnp
is mentioned by
dbSNPrs121908657
ebirs121908657
HLIrs121908657
Exacrs121908657
Varsomers121908657
Maprs121908657
PheGenIrs121908657
hapmaprs121908657
1000 genomesrs121908657
hgdprs121908657
ensemblrs121908657
gopubmedrs121908657
geneviewrs121908657
scholarrs121908657
googlers121908657
pharmgkbrs121908657
gwascentralrs121908657
openSNPrs121908657
23andMers121908657
23andMe allrs121908657
SNP Nexus

SNPshotrs121908657
SNPdbers121908657
MSV3drs121908657
GWAS Ctlgrs121908657
Max Magnitude0
OMIM603499
Desc
Variant0005
Relatedalso
ClinVar
Risk rs121908657(T;T)
Alt rs121908657(T;T)
Reference rs121908657(C;C)
Significance Pathogenic
Disease Osteopetrosis autosomal recessive 7
Variation info
Gene TNFRSF11A
CLNDBN Osteopetrosis autosomal recessive 7
Reversed 0
HGVS NC_000018.9:g.60021725C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000006683.3,