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rs121908656

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121908656(C;C)
Make rs121908656(C;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position62359956
GeneTNFRSF11A
is asnp
is mentioned by
dbSNPrs121908656
ebirs121908656
HLIrs121908656
Exacrs121908656
Varsomers121908656
Maprs121908656
PheGenIrs121908656
hapmaprs121908656
1000 genomesrs121908656
hgdprs121908656
ensemblrs121908656
gopubmedrs121908656
geneviewrs121908656
scholarrs121908656
googlers121908656
pharmgkbrs121908656
gwascentralrs121908656
openSNPrs121908656
23andMers121908656
23andMe allrs121908656
SNP Nexus

SNPshotrs121908656
SNPdbers121908656
MSV3drs121908656
GWAS Ctlgrs121908656
Max Magnitude0
OMIM603499
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121908656(C;C)
Alt rs121908656(C;C)
Reference rs121908656(T;T)
Significance Pathogenic
Disease Osteopetrosis autosomal recessive 7
Variation info
Gene TNFRSF11A
CLNDBN Osteopetrosis autosomal recessive 7
Reversed 0
HGVS NC_000018.9:g.60027189T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000006682.2,