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rs6927172

From SNPedia

Orientationplus
Stabilizedplus
Make rs6927172(C;C)
Make rs6927172(C;G)
Make rs6927172(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position137681038
is asnp
is mentioned by
dbSNPrs6927172
dbSNP (classic)rs6927172
ClinGenrs6927172
ebirs6927172
HLIrs6927172
Exacrs6927172
Gnomadrs6927172
Varsomers6927172
LitVarrs6927172
Maprs6927172
PheGenIrs6927172
Biobankrs6927172
1000 genomesrs6927172
hgdprs6927172
ensemblrs6927172
geneviewrs6927172
scholarrs6927172
googlers6927172
pharmgkbrs6927172
gwascentralrs6927172
openSNPrs6927172
23andMers6927172
SNPshotrs6927172
SNPdbers6927172
MSV3drs6927172
GWAS Ctlgrs6927172
Max Magnitude0
? (C;C) (C;G) (G;G) 28


[PMID 24776844] Associations between functional polymorphisms in the NFκB signaling pathway and response to anti-TNF treatment in Danish patients with inflammatory bowel disease


[PMID 27799070OA-icon.png] Capture Hi-C identifies a novel causal gene, IL20RA, in the pan-autoimmune genetic susceptibility region 6q23.