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rs251253

From SNPedia

Orientationminus
Stabilizedminus
Make rs251253(A;A)
Make rs251253(A;G)
Make rs251253(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position173053333
is asnp
is mentioned by
dbSNPrs251253
ebirs251253
HLIrs251253
Exacrs251253
Varsomers251253
Maprs251253
PheGenIrs251253
hapmaprs251253
1000 genomesrs251253
hgdprs251253
ensemblrs251253
gopubmedrs251253
geneviewrs251253
scholarrs251253
googlers251253
pharmgkbrs251253
gwascentralrs251253
openSNPrs251253
23andMers251253
23andMe allrs251253
SNP Nexus

SNPshotrs251253
SNPdbers251253
MSV3drs251253
GWAS Ctlgrs251253
GMAF0.4187
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 20062060OA-icon.png]
Trait PR interval
Title Genome-wide association study of PR interval
Risk Allele C
P-val 9E-13
Odds Ratio 1.49 [1.08-1.90] ms decrease


[PMID 21347284OA-icon.png] Genome-wide association studies of the PR interval in African Americans.


[PMID 24922963] 163 Genetic Modifiers in Carriers of the SCN5A E1784K Mutation with Variable Phenotypic Expression - Long QT3 / Brugada Syndrome Overlap Disease