Have questions? Visit https://www.reddit.com/r/SNPedia

rs2670321

From SNPedia

Orientationplus
Stabilizedplus
Make rs2670321(A;A)
Make rs2670321(A;C)
Make rs2670321(C;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position99448263
is asnp
is mentioned by
dbSNPrs2670321
ebirs2670321
HLIrs2670321
Exacrs2670321
Varsomers2670321
Maprs2670321
PheGenIrs2670321
hapmaprs2670321
1000 genomesrs2670321
hgdprs2670321
ensemblrs2670321
gopubmedrs2670321
geneviewrs2670321
scholarrs2670321
googlers2670321
pharmgkbrs2670321
gwascentralrs2670321
openSNPrs2670321
23andMers2670321
23andMe allrs2670321
SNP Nexus

SNPshotrs2670321
SNPdbers2670321
MSV3drs2670321
GWAS Ctlgrs2670321
GMAF0.4096
Max Magnitude
? (A;A) (A;C) (C;C) 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 C
P-val 0.000002
Odds Ratio 0.16 [0.10-0.22] unit decrease


GET Evidence
rs2670321
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.445312
summary