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rs879253796

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
(C;C) 0 common in clinvar
Make rs879253796(-;-)
Make rs879253796(-;CTGCTCTGCGCGCTGCTC)
Make rs879253796(CTGCTCTGCGCGCTGCTC;CTGCTCTGCGCGCTGCTC)
ReferenceGRCh38.p2 38.2/147
Chromosome18
Position62325415
GeneTNFRSF11A
is asnp
is mentioned by
dbSNPrs879253796
ebirs879253796
HLIrs879253796
Exacrs879253796
Varsomers879253796
Maprs879253796
PheGenIrs879253796
hapmaprs879253796
1000 genomesrs879253796
hgdprs879253796
ensemblrs879253796
gopubmedrs879253796
geneviewrs879253796
scholarrs879253796
googlers879253796
pharmgkbrs879253796
gwascentralrs879253796
openSNPrs879253796
23andMers879253796
23andMe allrs879253796
SNP Nexus

SNPshotrs879253796
SNPdbers879253796
MSV3drs879253796
GWAS Ctlgrs879253796
Max Magnitude0
ClinVar
Risk rs879253796(CCTCTGCGCGCTGCTC;CCTCTGCGCGCTGCTC) rs879253796(CCTGCTCTGCGCGCTGCTC;CCTGCTCTGCGCGCTGCTC)
Alt rs879253796(CCTCTGCGCGCTGCTC;CCTCTGCGCGCTGCTC) rs879253796(CCTGCTCTGCGCGCTGCTC;CCTGCTCTGCGCGCTGCTC)
Reference Rs879253796(C;C)
Significance Pathogenic
Disease Familial expansile osteolysis Paget disease of bone 2
Variation info
Gene TNFRSF11A
CLNDBN Familial expansile osteolysis Paget disease of bone 2, early-onset
Reversed 0
HGVS NC_000018.9:g.59992631_59992648dup18; NC_000018.9:g.59992634_59992648dupCTCTGCGCGCTGCTC
CLNSRC OMIM Allelic Variant
CLNACC RCV000006679.4, RCV000190352.2,