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rs760011764

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs760011764(A;G)
Make rs760011764(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position38613766
GeneSCN5A
is asnp
is mentioned by
dbSNPrs760011764
ebirs760011764
HLIrs760011764
Exacrs760011764
Varsomers760011764
Maprs760011764
PheGenIrs760011764
hapmaprs760011764
1000 genomesrs760011764
hgdprs760011764
ensemblrs760011764
gopubmedrs760011764
geneviewrs760011764
scholarrs760011764
googlers760011764
pharmgkbrs760011764
gwascentralrs760011764
openSNPrs760011764
23andMers760011764
23andMe allrs760011764
SNP Nexus

SNPshotrs760011764
SNPdbers760011764
MSV3drs760011764
GWAS Ctlgrs760011764
Max Magnitude0
ClinVar
Risk rs760011764(G;G)
Alt rs760011764(G;G)
Reference rs760011764(A;A)
Significance Probable-Pathogenic
Disease not provided not specified Brugada syndrome
Variation info
Gene SCN5A
CLNDBN not provided not specified Brugada syndrome
Reversed 0
HGVS NC_000003.11:g.38655257A>G
CLNSRC
CLNACC RCV000182943.2, RCV000223856.1, RCV000229800.1,