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rs199473255

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199473255(A;G)
Make rs199473255(G;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38556463
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473255
ebirs199473255
HLIrs199473255
Exacrs199473255
Varsomers199473255
Maprs199473255
PheGenIrs199473255
hapmaprs199473255
1000 genomesrs199473255
hgdprs199473255
ensemblrs199473255
gopubmedrs199473255
geneviewrs199473255
scholarrs199473255
googlers199473255
pharmgkbrs199473255
gwascentralrs199473255
openSNPrs199473255
23andMers199473255
23andMe allrs199473255
SNP Nexus

SNPshotrs199473255
SNPdbers199473255
MSV3drs199473255
GWAS Ctlgrs199473255
Max Magnitude0
ClinVar
Risk rs199473255(G;G)
Alt rs199473255(G;G)
Reference rs199473255(A;A)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene SCN5A
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000003.11:g.38597954T>C
CLNSRC ClinVar
CLNACC RCV000058670.2,