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rs4491792

From SNPedia

Orientationplus
Stabilizedplus
Make rs4491792(C;C)
Make rs4491792(C;T)
Make rs4491792(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position16760180
is asnp
is mentioned by
dbSNPrs4491792
dbSNP (classic)rs4491792
ClinGenrs4491792
ebirs4491792
HLIrs4491792
Exacrs4491792
Gnomadrs4491792
Varsomers4491792
LitVarrs4491792
Maprs4491792
PheGenIrs4491792
Biobankrs4491792
1000 genomesrs4491792
hgdprs4491792
ensemblrs4491792
geneviewrs4491792
scholarrs4491792
googlers4491792
pharmgkbrs4491792
gwascentralrs4491792
openSNPrs4491792
23andMers4491792
SNPshotrs4491792
SNPdbers4491792
MSV3drs4491792
GWAS Ctlgrs4491792
GMAF0.2443
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 23726511OA-icon.png]
Trait Post-traumatic stress disorder (asjusted for relatedness)
Title Genome-wide Association Study Identifies New Susceptibility Loci for Posttraumatic Stress Disorder.
Risk Allele
P-val 4E-6
Odds Ratio NR NR