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rs2731006

From SNPedia

Orientationplus
Stabilizedplus
Make rs2731006(C;C)
Make rs2731006(C;T)
Make rs2731006(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position42767023
is asnp
is mentioned by
dbSNPrs2731006
ebirs2731006
HLIrs2731006
Exacrs2731006
Varsomers2731006
Maprs2731006
PheGenIrs2731006
hapmaprs2731006
1000 genomesrs2731006
hgdprs2731006
ensemblrs2731006
gopubmedrs2731006
geneviewrs2731006
scholarrs2731006
googlers2731006
pharmgkbrs2731006
gwascentralrs2731006
openSNPrs2731006
23andMers2731006
23andMe allrs2731006
SNP Nexus

SNPshotrs2731006
SNPdbers2731006
MSV3drs2731006
GWAS Ctlgrs2731006
GMAF0.1635
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19165232]
Trait Panic disorder
Title Genome-wide association study of panic disorder in the Japanese population
Risk Allele
P-val 0.000004
Odds Ratio NR NR



GET Evidence
rs2731006
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.125
summary