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rs199473101

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473101(A;A)
Make rs199473101(A;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38606682
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473101
ebirs199473101
HLIrs199473101
Exacrs199473101
Varsomers199473101
Maprs199473101
PheGenIrs199473101
hapmaprs199473101
1000 genomesrs199473101
hgdprs199473101
ensemblrs199473101
gopubmedrs199473101
geneviewrs199473101
scholarrs199473101
googlers199473101
pharmgkbrs199473101
gwascentralrs199473101
openSNPrs199473101
23andMers199473101
23andMe allrs199473101
SNP Nexus

SNPshotrs199473101
SNPdbers199473101
MSV3drs199473101
GWAS Ctlgrs199473101
Max Magnitude0
ClinVar
Risk rs199473101(A;A)
Alt rs199473101(A;A)
Reference rs199473101(G;G)
Significance Pathogenic
Disease Brugada syndrome not provided
Variation info
Gene SCN5A
CLNDBN Brugada syndrome not provided
Reversed 1
HGVS NC_000003.11:g.38648173C>T
CLNSRC ClinVar
CLNACC RCV000058396.2, RCV000182960.2,