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rs199473071

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473071(A;A)
Make rs199473071(A;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38613772
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473071
dbSNP (old)rs199473071
ClinGenrs199473071
ebirs199473071
HLIrs199473071
Exacrs199473071
Gnomadrs199473071
Varsomers199473071
Maprs199473071
PheGenIrs199473071
Biobankrs199473071
1000 genomesrs199473071
hgdprs199473071
ensemblrs199473071
gopubmedrs199473071
geneviewrs199473071
scholarrs199473071
googlers199473071
pharmgkbrs199473071
gwascentralrs199473071
openSNPrs199473071
23andMers199473071
23andMe allrs199473071
SNP Nexus

SNPshotrs199473071
SNPdbers199473071
MSV3drs199473071
GWAS Ctlgrs199473071
Max Magnitude0
ClinVar
Risk rs199473071(A;A)
Alt rs199473071(A;A)
Reference Rs199473071(G;G)
Significance Untested
Disease Congenital long QT syndrome
Variation info
Gene SCN5A
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000003.11:g.38655263C>T
CLNSRC UniProtKB (protein)
CLNACC RCV000058836.3,