Have questions? Visit https://www.reddit.com/r/SNPedia

rs199473325

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473325(A;A)
Make rs199473325(A;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38550671
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473325
ebirs199473325
HLIrs199473325
Exacrs199473325
Varsomers199473325
Maprs199473325
PheGenIrs199473325
hapmaprs199473325
1000 genomesrs199473325
hgdprs199473325
ensemblrs199473325
gopubmedrs199473325
geneviewrs199473325
scholarrs199473325
googlers199473325
pharmgkbrs199473325
gwascentralrs199473325
openSNPrs199473325
23andMers199473325
23andMe allrs199473325
SNP Nexus

SNPshotrs199473325
SNPdbers199473325
MSV3drs199473325
GWAS Ctlgrs199473325
Max Magnitude0
ClinVar
Risk rs199473325(A,C;A,C)
Alt rs199473325(A,C;A,C)
Reference rs199473325(G;G)
Significance Pathogenic
Disease Congenital long QT syndrome not provided
Variation info
Gene SCN5A
CLNDBN Congenital long QT syndrome not provided
Reversed 1
HGVS NC_000003.11:g.38592162C>G; NC_000003.11:g.38592162C>T
CLNSRC ClinVar
CLNACC RCV000058801.2, RCV000058800.2,