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rs876661031

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876661031(A;A)
Make rs876661031(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position6333742
GeneTNFRSF1A
is asnp
is mentioned by
dbSNPrs876661031
ebirs876661031
HLIrs876661031
Exacrs876661031
Varsomers876661031
Maprs876661031
PheGenIrs876661031
hapmaprs876661031
1000 genomesrs876661031
hgdprs876661031
ensemblrs876661031
gopubmedrs876661031
geneviewrs876661031
scholarrs876661031
googlers876661031
pharmgkbrs876661031
gwascentralrs876661031
openSNPrs876661031
23andMers876661031
23andMe allrs876661031
SNP Nexus

SNPshotrs876661031
SNPdbers876661031
MSV3drs876661031
GWAS Ctlgrs876661031
Max Magnitude0
ClinVar
Risk rs876661031(A;A)
Alt rs876661031(A;A)
Reference rs876661031(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TNFRSF1A
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.6442908C>T
CLNSRC
CLNACC RCV000216297.1,