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rs4702982

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs4702982(C;T)
Make rs4702982(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position100655944
is asnp
is mentioned by
dbSNPrs4702982
ebirs4702982
HLIrs4702982
Exacrs4702982
Varsomers4702982
Maprs4702982
PheGenIrs4702982
hapmaprs4702982
1000 genomesrs4702982
hgdprs4702982
ensemblrs4702982
gopubmedrs4702982
geneviewrs4702982
scholarrs4702982
googlers4702982
pharmgkbrs4702982
gwascentralrs4702982
openSNPrs4702982
23andMers4702982
23andMe allrs4702982
SNP Nexus

SNPshotrs4702982
SNPdbers4702982
MSV3drs4702982
GWAS Ctlgrs4702982
GMAF0.1295
Max Magnitude0
? (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 0.000006
Odds Ratio NR NR



GET Evidence
rs4702982
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.125
summary