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rs737582

From SNPedia

Orientationminus
Stabilizedminus
Make rs737582(C;C)
Make rs737582(C;T)
Make rs737582(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position99992669
GeneCNTN5
is asnp
is mentioned by
dbSNPrs737582
ebirs737582
HLIrs737582
Exacrs737582
Varsomers737582
Maprs737582
PheGenIrs737582
hapmaprs737582
1000 genomesrs737582
hgdprs737582
ensemblrs737582
gopubmedrs737582
geneviewrs737582
scholarrs737582
googlers737582
pharmgkbrs737582
gwascentralrs737582
openSNPrs737582
23andMers737582
23andMe allrs737582
SNP Nexus

SNPshotrs737582
SNPdbers737582
MSV3drs737582
GWAS Ctlgrs737582
GMAF0.3365
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 19680270] Identification of novel candidate loci for anorexia nervosa at 1q41 and 11q22 in Japanese by a genome-wide association analysis with microsatellite markers



GET Evidence
rs737582
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.390625
summary