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rs9352774

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs9352774(A;C)
Make rs9352774(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position63304907
GeneLGSN
is asnp
is mentioned by
dbSNPrs9352774
ebirs9352774
HLIrs9352774
Exacrs9352774
Varsomers9352774
Maprs9352774
PheGenIrs9352774
hapmaprs9352774
1000 genomesrs9352774
hgdprs9352774
ensemblrs9352774
gopubmedrs9352774
geneviewrs9352774
scholarrs9352774
googlers9352774
pharmgkbrs9352774
gwascentralrs9352774
openSNPrs9352774
23andMers9352774
23andMe allrs9352774
SNP Nexus

SNPshotrs9352774
SNPdbers9352774
MSV3drs9352774
GWAS Ctlgrs9352774
GMAF0.1203
Max Magnitude0
? (A;A) (A;C) (C;C) 28

[PMID 21621269] Genome-wide association analysis of gender differences in major depressive disorder in the Netherlands NESDA and NTR population-based samples