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rs184442491

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs184442491(A;A)
Make rs184442491(A;C)
ReferenceGRCh38 38.1/142
Chromosome3
Position38603888
GeneSCN5A
is asnp
is mentioned by
dbSNPrs184442491
ebirs184442491
HLIrs184442491
Exacrs184442491
Varsomers184442491
Maprs184442491
PheGenIrs184442491
hapmaprs184442491
1000 genomesrs184442491
hgdprs184442491
ensemblrs184442491
gopubmedrs184442491
geneviewrs184442491
scholarrs184442491
googlers184442491
pharmgkbrs184442491
gwascentralrs184442491
openSNPrs184442491
23andMers184442491
23andMe allrs184442491
SNP Nexus

SNPshotrs184442491
SNPdbers184442491
MSV3drs184442491
GWAS Ctlgrs184442491
Max Magnitude0
ClinVar
Risk rs184442491(A;A)
Alt rs184442491(A;A)
Reference rs184442491(C;C)
Significance Pathogenic
Disease Congenital long QT syndrome Long QT syndrome
Variation info
Gene SCN5A
CLNDBN Congenital long QT syndrome Long QT syndrome
Reversed 0
HGVS NC_000003.11:g.38645379C>A
CLNSRC ClinVar University of Washington
CLNACC RCV000058446.2, RCV000148854.1,