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rs1484948

From SNPedia

Orientationplus
Stabilizedplus
Make rs1484948(C;C)
Make rs1484948(C;T)
Make rs1484948(T;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position41831114
GeneLINC01499
is asnp
is mentioned by
dbSNPrs1484948
ebirs1484948
HLIrs1484948
Exacrs1484948
Varsomers1484948
Maprs1484948
PheGenIrs1484948
hapmaprs1484948
1000 genomesrs1484948
hgdprs1484948
ensemblrs1484948
gopubmedrs1484948
geneviewrs1484948
scholarrs1484948
googlers1484948
pharmgkbrs1484948
gwascentralrs1484948
openSNPrs1484948
23andMers1484948
23andMe allrs1484948
SNP Nexus

SNPshotrs1484948
SNPdbers1484948
MSV3drs1484948
GWAS Ctlgrs1484948
GMAF0.2011
Max Magnitude
? (C;C) (C;T) (T;T) 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 G
P-val 0.000002
Odds Ratio 0.16 [0.10-0.22] unit increase


GET Evidence
rs1484948
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.234375
summary