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rs96844

From SNPedia

Orientationminus
Stabilizedminus
Make rs96844(C;C)
Make rs96844(C;T)
Make rs96844(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position56900777
is asnp
is mentioned by
dbSNPrs96844
ebirs96844
HLIrs96844
Exacrs96844
Varsomers96844
Maprs96844
PheGenIrs96844
hapmaprs96844
1000 genomesrs96844
hgdprs96844
ensemblrs96844
gopubmedrs96844
geneviewrs96844
scholarrs96844
googlers96844
pharmgkbrs96844
gwascentralrs96844
openSNPrs96844
23andMers96844
23andMe allrs96844
SNP Nexus

SNPshotrs96844
SNPdbers96844
MSV3drs96844
GWAS Ctlgrs96844
GMAF0.4798
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 19262425] Investigation of genetic variants within candidate genes of the TNFRSF1B signalling pathway on the response to anti-TNF agents in a UK cohort of rheumatoid arthritis patients