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rs201641342

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs201641342(A;A)
Make rs201641342(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position38603950
GeneSCN5A
is asnp
is mentioned by
dbSNPrs201641342
ebirs201641342
HLIrs201641342
Exacrs201641342
Varsomers201641342
Maprs201641342
PheGenIrs201641342
hapmaprs201641342
1000 genomesrs201641342
hgdprs201641342
ensemblrs201641342
gopubmedrs201641342
geneviewrs201641342
scholarrs201641342
googlers201641342
pharmgkbrs201641342
gwascentralrs201641342
openSNPrs201641342
23andMers201641342
23andMe allrs201641342
SNP Nexus

SNPshotrs201641342
SNPdbers201641342
MSV3drs201641342
GWAS Ctlgrs201641342
Max Magnitude0
ClinVar
Risk rs201641342(A;A)
Alt rs201641342(A;A)
Reference rs201641342(G;G)
Significance Probable-Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 0
HGVS NC_000003.11:g.38645441G>A
CLNSRC
CLNACC RCV000171573.1,