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rs192113333

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs192113333(C;T)
Make rs192113333(T;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38620901
GeneSCN5A
is asnp
is mentioned by
dbSNPrs192113333
ebirs192113333
HLIrs192113333
Exacrs192113333
Varsomers192113333
Maprs192113333
PheGenIrs192113333
hapmaprs192113333
1000 genomesrs192113333
hgdprs192113333
ensemblrs192113333
gopubmedrs192113333
geneviewrs192113333
scholarrs192113333
googlers192113333
pharmgkbrs192113333
gwascentralrs192113333
openSNPrs192113333
23andMers192113333
23andMe allrs192113333
SNP Nexus

SNPshotrs192113333
SNPdbers192113333
MSV3drs192113333
GWAS Ctlgrs192113333
Max Magnitude0
ClinVar
Risk rs192113333(T;T)
Alt rs192113333(T;T)
Reference rs192113333(C;C)
Significance Pathogenic
Disease Congenital long QT syndrome not provided
Variation info
Gene SCN5A
CLNDBN Congenital long QT syndrome not provided
Reversed 0
HGVS NC_000003.11:g.38662392C>T
CLNSRC ClinVar
CLNACC RCV000058790.2, RCV000182931.2,