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rs199473099

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473099(C;T)
Make rs199473099(T;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38606700
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473099
ebirs199473099
HLIrs199473099
Exacrs199473099
Varsomers199473099
Maprs199473099
PheGenIrs199473099
hapmaprs199473099
1000 genomesrs199473099
hgdprs199473099
ensemblrs199473099
gopubmedrs199473099
geneviewrs199473099
scholarrs199473099
googlers199473099
pharmgkbrs199473099
gwascentralrs199473099
openSNPrs199473099
23andMers199473099
23andMe allrs199473099
SNP Nexus

SNPshotrs199473099
SNPdbers199473099
MSV3drs199473099
GWAS Ctlgrs199473099
Max Magnitude0
ClinVar
Risk rs199473099(T;T)
Alt rs199473099(T;T)
Reference rs199473099(C;C)
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.38648191G>A
CLNSRC ClinVar
CLNACC RCV000058393.2, RCV000182959.2,