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rs199473106

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473106(C;C)
Make rs199473106(C;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38606090
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473106
ebirs199473106
HLIrs199473106
Exacrs199473106
Varsomers199473106
Maprs199473106
PheGenIrs199473106
hapmaprs199473106
1000 genomesrs199473106
hgdprs199473106
ensemblrs199473106
gopubmedrs199473106
geneviewrs199473106
scholarrs199473106
googlers199473106
pharmgkbrs199473106
gwascentralrs199473106
openSNPrs199473106
23andMers199473106
23andMe allrs199473106
SNP Nexus

SNPshotrs199473106
SNPdbers199473106
MSV3drs199473106
GWAS Ctlgrs199473106
Max Magnitude0
ClinVar
Risk rs199473106(C;C)
Alt rs199473106(C;C)
Reference rs199473106(G;G)
Significance Pathogenic
Disease Ventricular fibrillation
Variation info
Gene SCN5A
CLNDBN Ventricular fibrillation
Reversed 1
HGVS NC_000003.11:g.38647581C>G
CLNSRC ClinVar
CLNACC RCV000058402.2,