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rs2099684

From SNPedia

Orientationplus
Stabilizedplus
Make rs2099684(A;A)
Make rs2099684(A;G)
Make rs2099684(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position161530340
is asnp
is mentioned by
dbSNPrs2099684
dbSNP (classic)rs2099684
ClinGenrs2099684
ebirs2099684
HLIrs2099684
Exacrs2099684
Gnomadrs2099684
Varsomers2099684
LitVarrs2099684
Maprs2099684
PheGenIrs2099684
Biobankrs2099684
1000 genomesrs2099684
hgdprs2099684
ensemblrs2099684
geneviewrs2099684
scholarrs2099684
googlers2099684
pharmgkbrs2099684
gwascentralrs2099684
openSNPrs2099684
23andMers2099684
23andMe allrs2099684
SNPshotrs2099684
SNPdbers2099684
MSV3drs2099684
GWAS Ctlgrs2099684
Max Magnitude0
? (A;A) (A;G) (G;G) 28


[PMID 27769046OA-icon.png] Association of FCGR2A/FCGR3A variant rs2099684 with Takayasu arteritis in the Han Chinese population.