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rs17608766

From SNPedia

Orientationplus
Stabilizedplus
Make rs17608766(C;C)
Make rs17608766(C;T)
Make rs17608766(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position46935905
GeneGOSR2
is asnp
is mentioned by
dbSNPrs17608766
ebirs17608766
HLIrs17608766
Exacrs17608766
Varsomers17608766
Maprs17608766
PheGenIrs17608766
hapmaprs17608766
1000 genomesrs17608766
hgdprs17608766
ensemblrs17608766
gopubmedrs17608766
geneviewrs17608766
scholarrs17608766
googlers17608766
pharmgkbrs17608766
gwascentralrs17608766
openSNPrs17608766
23andMers17608766
23andMe allrs17608766
SNP Nexus

SNPshotrs17608766
SNPdbers17608766
MSV3drs17608766
GWAS Ctlgrs17608766
GMAF0.07254
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21076409OA-icon.png]
Trait
Title Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction
Risk Allele C
P-val 5E-10
Odds Ratio 0.5300 [0.33-0.73] ms increase
GWAS snp
PMID [PMID 21909115OA-icon.png]
Trait
Title Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.
Risk Allele T
P-val 1E-10
Odds Ratio 0.5560 [NR] mmHg decrease
GWAS snp
PMID [PMID 21909110OA-icon.png]
Trait
Title Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.
Risk Allele T
P-val 2E-7
Odds Ratio 0.3640 [0.23-0.50] mmHg decrease


[PMID 23313660] A haplotype of the GOSR2 gene is associated with essential hypertension in Japanese men.


[PMID 23675987OA-icon.png] A haplotype of the GOSR2 gene is associated with myocardial infarction in Japanese men.