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rs199473165

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199473165(A;G)
Make rs199473165(G;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38585951
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473165
ebirs199473165
HLIrs199473165
Exacrs199473165
Varsomers199473165
Maprs199473165
PheGenIrs199473165
hapmaprs199473165
1000 genomesrs199473165
hgdprs199473165
ensemblrs199473165
gopubmedrs199473165
geneviewrs199473165
scholarrs199473165
googlers199473165
pharmgkbrs199473165
gwascentralrs199473165
openSNPrs199473165
23andMers199473165
23andMe allrs199473165
SNP Nexus

SNPshotrs199473165
SNPdbers199473165
MSV3drs199473165
GWAS Ctlgrs199473165
Max Magnitude0
ClinVar
Risk rs199473165(G;G)
Alt rs199473165(G;G)
Reference rs199473165(A;A)
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.38627442T>C
CLNSRC ClinVar
CLNACC RCV000058508.2, RCV000183178.1,