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rs9260997

From SNPedia

Orientationplus
Stabilizedplus
Make rs9260997(C;C)
Make rs9260997(C;T)
Make rs9260997(T;T)
ReferenceGRCh38 38.1/142
Chromosome6
Position29995539
is asnp
is mentioned by
dbSNPrs9260997
ebirs9260997
HLIrs9260997
Exacrs9260997
Varsomers9260997
Maprs9260997
PheGenIrs9260997
hapmaprs9260997
1000 genomesrs9260997
hgdprs9260997
ensemblrs9260997
gopubmedrs9260997
geneviewrs9260997
scholarrs9260997
googlers9260997
pharmgkbrs9260997
gwascentralrs9260997
openSNPrs9260997
23andMers9260997
23andMe allrs9260997
SNP Nexus

SNPshotrs9260997
SNPdbers9260997
MSV3drs9260997
GWAS Ctlgrs9260997
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 25889189OA-icon.png] Characterization of the major histocompatibility complex locus association with Behçet's disease in Iran