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rs11848785

From SNPedia

Orientationplus
Stabilizedplus
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
dbSNP (classic)rs11848785
ClinGenrs11848785
ebirs11848785
HLIrs11848785
Exacrs11848785
Gnomadrs11848785
Varsomers11848785
LitVarrs11848785
Maprs11848785
PheGenIrs11848785
Biobankrs11848785
1000 genomesrs11848785
hgdprs11848785
ensemblrs11848785
geneviewrs11848785
scholarrs11848785
googlers11848785
pharmgkbrs11848785
gwascentralrs11848785
openSNPrs11848785
23andMers11848785
SNPshotrs11848785
SNPdbers11848785
MSV3drs11848785
GWAS Ctlgrs11848785
GMAF0.1556
Max Magnitude0
? (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