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rs876661014

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876661014(C;G)
Make rs876661014(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position6333777
GeneTNFRSF1A
is asnp
is mentioned by
dbSNPrs876661014
ebirs876661014
HLIrs876661014
Exacrs876661014
Varsomers876661014
Maprs876661014
PheGenIrs876661014
hapmaprs876661014
1000 genomesrs876661014
hgdprs876661014
ensemblrs876661014
gopubmedrs876661014
geneviewrs876661014
scholarrs876661014
googlers876661014
pharmgkbrs876661014
gwascentralrs876661014
openSNPrs876661014
23andMers876661014
23andMe allrs876661014
SNP Nexus

SNPshotrs876661014
SNPdbers876661014
MSV3drs876661014
GWAS Ctlgrs876661014
Max Magnitude0
ClinVar
Risk rs876661014(G;G)
Alt rs876661014(G;G)
Reference rs876661014(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TNFRSF1A
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.6442943G>C
CLNSRC
CLNACC RCV000218061.1,