Have questions? Visit https://www.reddit.com/r/SNPedia

rs2061634

From SNPedia

Orientationminus
Stabilizedminus
Make rs2061634(C;C)
Make rs2061634(C;G)
Make rs2061634(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position97343500
GeneBDAG1, C9orf174
is asnp
is mentioned by
dbSNPrs2061634
ebirs2061634
HLIrs2061634
Exacrs2061634
Varsomers2061634
Maprs2061634
PheGenIrs2061634
hapmaprs2061634
1000 genomesrs2061634
hgdprs2061634
ensemblrs2061634
gopubmedrs2061634
geneviewrs2061634
scholarrs2061634
googlers2061634
pharmgkbrs2061634
gwascentralrs2061634
openSNPrs2061634
23andMers2061634
23andMe allrs2061634
SNP Nexus

SNPshotrs2061634
SNPdbers2061634
MSV3drs2061634
GWAS Ctlgrs2061634
GMAF0.2479
Max Magnitude
? (C;C) (C;G) (G;G) 28
[PMID 19442274OA-icon.png] First genome-wide association study for this disorder, albeit of 152 patients, reports an association between this SNP (odds ratio 2.04, p = 4.2 x10e-5) and Behcet's disease.


GET Evidence
C9ORF174-S995C
aa_change Ser995Cys
aa_change_short S995C
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.324596
summary