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rs17706439

From SNPedia

Orientationplus
Stabilizedplus
Make rs17706439(A;A)
Make rs17706439(A;G)
Make rs17706439(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position213682245
is asnp
is mentioned by
dbSNPrs17706439
ebirs17706439
HLIrs17706439
Exacrs17706439
Varsomers17706439
Maprs17706439
PheGenIrs17706439
hapmaprs17706439
1000 genomesrs17706439
hgdprs17706439
ensemblrs17706439
gopubmedrs17706439
geneviewrs17706439
scholarrs17706439
googlers17706439
pharmgkbrs17706439
gwascentralrs17706439
openSNPrs17706439
23andMers17706439
23andMe allrs17706439
SNP Nexus

SNPshotrs17706439
SNPdbers17706439
MSV3drs17706439
GWAS Ctlgrs17706439
GMAF0.1001
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 20031603OA-icon.png]
Trait RR interval (heart rate)
Title A Genome-Wide Association Scan of RR and QT Interval Duration in 3 European Genetically Isolated Populations: The EUROSPAN Project
Risk Allele A
P-val 0.000003
Odds Ratio 0.18 [0.10-0.26] unit increase


GET Evidence
rs17706439
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.109375
summary