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rs786205594

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205594(G;T)
Make rs786205594(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position118933137
GeneTNFRSF11B
is asnp
is mentioned by
dbSNPrs786205594
ebirs786205594
HLIrs786205594
Exacrs786205594
Varsomers786205594
Maprs786205594
PheGenIrs786205594
hapmaprs786205594
1000 genomesrs786205594
hgdprs786205594
ensemblrs786205594
gopubmedrs786205594
geneviewrs786205594
scholarrs786205594
googlers786205594
pharmgkbrs786205594
gwascentralrs786205594
openSNPrs786205594
23andMers786205594
23andMe allrs786205594
SNP Nexus

SNPshotrs786205594
SNPdbers786205594
MSV3drs786205594
GWAS Ctlgrs786205594
Max Magnitude0
ClinVar
Risk rs786205594(T;T)
Alt rs786205594(T;T)
Reference rs786205594(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TNFRSF11B
CLNDBN not provided
Reversed 1
HGVS NC_000008.10:g.119945376C>A
CLNSRC
CLNACC RCV000171419.1,