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rs7299940

From SNPedia

Orientationplus
Stabilizedplus
Make rs7299940(C;C)
Make rs7299940(C;G)
Make rs7299940(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position130906209
is asnp
is mentioned by
dbSNPrs7299940
ebirs7299940
HLIrs7299940
Exacrs7299940
Varsomers7299940
Maprs7299940
PheGenIrs7299940
hapmaprs7299940
1000 genomesrs7299940
hgdprs7299940
ensemblrs7299940
gopubmedrs7299940
geneviewrs7299940
scholarrs7299940
googlers7299940
pharmgkbrs7299940
gwascentralrs7299940
openSNPrs7299940
23andMers7299940
23andMe allrs7299940
SNP Nexus

SNPshotrs7299940
SNPdbers7299940
MSV3drs7299940
GWAS Ctlgrs7299940
GMAF0.4692
Max Magnitude
? (C;C) (C;G) (G;G) 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 0.000007
Odds Ratio NR NR



GET Evidence
rs7299940
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.570312
summary