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rs2848713

From SNPedia

Orientationplus
Stabilizedplus
Make rs2848713(A;A)
Make rs2848713(A;G)
Make rs2848713(G;G)
ReferenceGRCh38 38.1/142
Chromosome6
Position31416702
is asnp
is mentioned by
dbSNPrs2848713
dbSNP (classic)rs2848713
ClinGenrs2848713
ebirs2848713
HLIrs2848713
Exacrs2848713
Gnomadrs2848713
Varsomers2848713
LitVarrs2848713
Maprs2848713
PheGenIrs2848713
Biobankrs2848713
1000 genomesrs2848713
hgdprs2848713
ensemblrs2848713
geneviewrs2848713
scholarrs2848713
googlers2848713
pharmgkbrs2848713
gwascentralrs2848713
openSNPrs2848713
23andMers2848713
SNPshotrs2848713
SNPdbers2848713
MSV3drs2848713
GWAS Ctlgrs2848713
Max Magnitude0
? (A;A) (A;G) (G;G) 28


[PMID 25889189OA-icon.png] Characterization of the major histocompatibility complex locus association with Behçet's disease in Iran