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rs121908655

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121908655(A;G)
Make rs121908655(G;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position62358328
GeneTNFRSF11A
is asnp
is mentioned by
dbSNPrs121908655
ebirs121908655
HLIrs121908655
Exacrs121908655
Varsomers121908655
Maprs121908655
PheGenIrs121908655
hapmaprs121908655
1000 genomesrs121908655
hgdprs121908655
ensemblrs121908655
gopubmedrs121908655
geneviewrs121908655
scholarrs121908655
googlers121908655
pharmgkbrs121908655
gwascentralrs121908655
openSNPrs121908655
23andMers121908655
23andMe allrs121908655
SNP Nexus

SNPshotrs121908655
SNPdbers121908655
MSV3drs121908655
GWAS Ctlgrs121908655
Max Magnitude0
OMIM603499
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121908655(G;G)
Alt rs121908655(G;G)
Reference rs121908655(A;A)
Significance Pathogenic
Disease Osteopetrosis autosomal recessive 7
Variation info
Gene TNFRSF11A
CLNDBN Osteopetrosis autosomal recessive 7
Reversed 0
HGVS NC_000018.9:g.60025561A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000006681.2,