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rs7725217

From SNPedia

Orientationplus
Stabilizedplus
Make rs7725217(A;A)
Make rs7725217(A;C)
Make rs7725217(C;C)
ReferenceGRCh38 38.1/141
Chromosome5
Position9756217
GeneLOC105374649, LOC285692
is asnp
is mentioned by
dbSNPrs7725217
dbSNP (classic)rs7725217
ClinGenrs7725217
ebirs7725217
HLIrs7725217
Exacrs7725217
Gnomadrs7725217
Varsomers7725217
LitVarrs7725217
Maprs7725217
PheGenIrs7725217
Biobankrs7725217
1000 genomesrs7725217
hgdprs7725217
ensemblrs7725217
geneviewrs7725217
scholarrs7725217
googlers7725217
pharmgkbrs7725217
gwascentralrs7725217
openSNPrs7725217
23andMers7725217
SNPshotrs7725217
SNPdbers7725217
MSV3drs7725217
GWAS Ctlgrs7725217
GMAF0.2231
Max Magnitude0
? (A;A) (A;C) (C;C) 28


GWAS snp
PMID [PMID 23646285OA-icon.png]
Trait Hypersomnia (HLA-DQB1*06:02 negative)
Title Genome-wide association study of HLA-DQB1*06:02 negative essential hypersomnia.
Risk Allele C
P-val 1E-6
Odds Ratio 2.66 [1.78-3.98]