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rs370694515

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs370694515(C;T)
Make rs370694515(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position38550679
GeneSCN5A
is asnp
is mentioned by
dbSNPrs370694515
ebirs370694515
HLIrs370694515
Exacrs370694515
Varsomers370694515
Maprs370694515
PheGenIrs370694515
hapmaprs370694515
1000 genomesrs370694515
hgdprs370694515
ensemblrs370694515
gopubmedrs370694515
geneviewrs370694515
scholarrs370694515
googlers370694515
pharmgkbrs370694515
gwascentralrs370694515
openSNPrs370694515
23andMers370694515
23andMe allrs370694515
SNP Nexus

SNPshotrs370694515
SNPdbers370694515
MSV3drs370694515
GWAS Ctlgrs370694515
Max Magnitude0
ClinVar
Risk rs370694515(T;T)
Alt rs370694515(T;T)
Reference rs370694515(C;C)
Significance Pathogenic
Disease not specified Long qt syndrome 3
Variation info
Gene SCN5A
CLNDBN not specified Long qt syndrome 3
Reversed 0
HGVS NC_000003.11:g.38592170C>T
CLNSRC
CLNACC RCV000216249.1, RCV000234809.1,