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rs199473258

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199473258(A;C)
Make rs199473258(C;C)
ReferenceGRCh38 38.1/142
Chromosome3
Position38555739
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473258
ebirs199473258
HLIrs199473258
Exacrs199473258
Varsomers199473258
Maprs199473258
PheGenIrs199473258
hapmaprs199473258
1000 genomesrs199473258
hgdprs199473258
ensemblrs199473258
gopubmedrs199473258
geneviewrs199473258
scholarrs199473258
googlers199473258
pharmgkbrs199473258
gwascentralrs199473258
openSNPrs199473258
23andMers199473258
23andMe allrs199473258
SNP Nexus

SNPshotrs199473258
SNPdbers199473258
MSV3drs199473258
GWAS Ctlgrs199473258
Max Magnitude0
ClinVar
Risk rs199473258(C;C)
Alt rs199473258(C;C)
Reference Rs199473258(A;A)
Significance Untested
Disease Congenital long QT syndrome
Variation info
Gene SCN5A
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000003.11:g.38597230T>G
CLNSRC ClinVar
CLNACC RCV000058675.3,