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rs4901869

From SNPedia

Orientationplus
Stabilizedplus
Make rs4901869(A;A)
Make rs4901869(A;G)
Make rs4901869(G;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position58867410
GeneLOC102723742
is asnp
is mentioned by
dbSNPrs4901869
ebirs4901869
HLIrs4901869
Exacrs4901869
Varsomers4901869
Maprs4901869
PheGenIrs4901869
hapmaprs4901869
1000 genomesrs4901869
hgdprs4901869
ensemblrs4901869
gopubmedrs4901869
geneviewrs4901869
scholarrs4901869
googlers4901869
pharmgkbrs4901869
gwascentralrs4901869
openSNPrs4901869
23andMers4901869
23andMe allrs4901869
SNP Nexus

SNPshotrs4901869
SNPdbers4901869
MSV3drs4901869
GWAS Ctlgrs4901869
GMAF0.2649
Max Magnitude
? (A;A) (A;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 0.000006
Odds Ratio NR NR



GET Evidence
rs4901869
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.288136
summary