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rs199473114

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199473114(A;C)
Make rs199473114(C;C)
ReferenceGRCh38 38.1/142
Chromosome3
Position38604862
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473114
ebirs199473114
HLIrs199473114
Exacrs199473114
Varsomers199473114
Maprs199473114
PheGenIrs199473114
hapmaprs199473114
1000 genomesrs199473114
hgdprs199473114
ensemblrs199473114
gopubmedrs199473114
geneviewrs199473114
scholarrs199473114
googlers199473114
pharmgkbrs199473114
gwascentralrs199473114
openSNPrs199473114
23andMers199473114
23andMe allrs199473114
SNP Nexus

SNPshotrs199473114
SNPdbers199473114
MSV3drs199473114
GWAS Ctlgrs199473114
Max Magnitude0
ClinVar
Risk rs199473114(C;C)
Alt rs199473114(C;C)
Reference rs199473114(A;A)
Significance Other
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.38646353T>G
CLNSRC ClinVar
CLNACC RCV000058420.2, RCV000174185.2,