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rs199473285

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473285(A;A)
Make rs199473285(A;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38551480
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473285
ebirs199473285
HLIrs199473285
Exacrs199473285
Varsomers199473285
Maprs199473285
PheGenIrs199473285
hapmaprs199473285
1000 genomesrs199473285
hgdprs199473285
ensemblrs199473285
gopubmedrs199473285
geneviewrs199473285
scholarrs199473285
googlers199473285
pharmgkbrs199473285
gwascentralrs199473285
openSNPrs199473285
23andMers199473285
23andMe allrs199473285
SNP Nexus

SNPshotrs199473285
SNPdbers199473285
MSV3drs199473285
GWAS Ctlgrs199473285
Max Magnitude0
ClinVar
Risk rs199473285(A;A)
Alt rs199473285(A;A)
Reference rs199473285(G;G)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene SCN5A
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000003.11:g.38592971C>T
CLNSRC ClinVar
CLNACC RCV000058722.2,