Rs11848785

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Orientationplus
Make rs11848785(A;A)
Make rs11848785(A;G)
Make rs11848785(G;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position71590638
GeneSIPA1L1
is asnp
is mentioned by
dbSNPrs11848785
PheGenIrs11848785
nextbiors11848785
hapmaprs11848785
1000 genomesrs11848785
hgdprs11848785
ensemblrs11848785
gopubmedrs11848785
geneviewrs11848785
scholarrs11848785
googlers11848785
pharmgkbrs11848785
gwascentralrs11848785
openSNPrs11848785
23andMers11848785
23andMe allrs11848785
SNP Nexus

SNPshotrs11848785
SNPdbers11848785
MSV3drs11848785
GMAF0.1556
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21076409OA-icon.png]
Trait
Title Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction
Risk Allele G
P-val 1E-10
Odds Ratio 0.5000 [0.34-0.66] ms decrease


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