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rs199473088

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473088(A;A)
Make rs199473088(A;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38609770
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473088
ebirs199473088
HLIrs199473088
Exacrs199473088
Varsomers199473088
Maprs199473088
PheGenIrs199473088
hapmaprs199473088
1000 genomesrs199473088
hgdprs199473088
ensemblrs199473088
gopubmedrs199473088
geneviewrs199473088
scholarrs199473088
googlers199473088
pharmgkbrs199473088
gwascentralrs199473088
openSNPrs199473088
23andMers199473088
23andMe allrs199473088
SNP Nexus

SNPshotrs199473088
SNPdbers199473088
MSV3drs199473088
GWAS Ctlgrs199473088
Max Magnitude0
ClinVar
Risk rs199473088(A;A)
Alt rs199473088(A;A)
Reference rs199473088(G;G)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38651261C>T
CLNSRC ClinVar
CLNACC RCV000058860.2,