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rs11129795

From SNPedia

Orientationplus
Stabilizedplus
Make rs11129795(A;A)
Make rs11129795(A;G)
Make rs11129795(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position38547672
GeneSCN5A
is asnp
is mentioned by
dbSNPrs11129795
ebirs11129795
HLIrs11129795
Exacrs11129795
Varsomers11129795
Maprs11129795
PheGenIrs11129795
hapmaprs11129795
1000 genomesrs11129795
hgdprs11129795
ensemblrs11129795
gopubmedrs11129795
geneviewrs11129795
scholarrs11129795
googlers11129795
pharmgkbrs11129795
gwascentralrs11129795
openSNPrs11129795
23andMers11129795
23andMe allrs11129795
SNP Nexus

SNPshotrs11129795
SNPdbers11129795
MSV3drs11129795
GWAS Ctlgrs11129795
GMAF0.2062
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19305409OA-icon.png]
Trait QT interval
Title Common variants at ten loci modulate the QT interval duration in the QTSCD Study
Risk Allele A
P-val 5E-14
Odds Ratio 1.27 [0.82-1.72] ms decrease


GWAS snp
PMID [PMID 20062063]
Trait Electrocardiographic traits
Title Several common variants modulate heart rate, PR interval and QRS duration
Risk Allele G
P-val 5E-10
Odds Ratio 8.24 [5.64-10.83] % SD decrease


[PMID 20062060OA-icon.png] Genome-wide association study of PR interval.


GET Evidence
rs11129795
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.226562
summary