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rs281865419

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281865419(C;T)
Make rs281865419(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31577157
GeneTNF
is asnp
is mentioned by
dbSNPrs281865419
ebirs281865419
HLIrs281865419
Exacrs281865419
Varsomers281865419
Maprs281865419
PheGenIrs281865419
hapmaprs281865419
1000 genomesrs281865419
hgdprs281865419
ensemblrs281865419
gopubmedrs281865419
geneviewrs281865419
scholarrs281865419
googlers281865419
pharmgkbrs281865419
gwascentralrs281865419
openSNPrs281865419
23andMers281865419
23andMe allrs281865419
SNP Nexus

SNPshotrs281865419
SNPdbers281865419
MSV3drs281865419
GWAS Ctlgrs281865419
Max Magnitude0
ClinVar
Risk rs281865419(T;T)
Alt rs281865419(T;T)
Reference rs281865419(C;C)
Significance Pathogenic
Disease TNF receptor binding
Variation info
Gene TNF
CLNDBN TNF receptor binding, altered
Reversed 0
HGVS NC_000006.11:g.31544934C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013187.24,