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rs199473075

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199473075(A;G)
Make rs199473075(G;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38609953
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473075
ebirs199473075
HLIrs199473075
Exacrs199473075
Varsomers199473075
Maprs199473075
PheGenIrs199473075
hapmaprs199473075
1000 genomesrs199473075
hgdprs199473075
ensemblrs199473075
gopubmedrs199473075
geneviewrs199473075
scholarrs199473075
googlers199473075
pharmgkbrs199473075
gwascentralrs199473075
openSNPrs199473075
23andMers199473075
23andMe allrs199473075
SNP Nexus

SNPshotrs199473075
SNPdbers199473075
MSV3drs199473075
GWAS Ctlgrs199473075
Max Magnitude0
ClinVar
Risk rs199473075(G;G)
Alt rs199473075(G;G)
Reference rs199473075(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.38651444T>C
CLNSRC ClinVar
CLNACC RCV000058841.2,