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rs36210420

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs36210420(A;C)
Make rs36210420(C;C)
ReferenceGRCh38 38.1/142
Chromosome3
Position38609797
GeneSCN5A
is asnp
is mentioned by
dbSNPrs36210420
ebirs36210420
HLIrs36210420
Exacrs36210420
Varsomers36210420
Maprs36210420
PheGenIrs36210420
hapmaprs36210420
1000 genomesrs36210420
hgdprs36210420
ensemblrs36210420
gopubmedrs36210420
geneviewrs36210420
scholarrs36210420
googlers36210420
pharmgkbrs36210420
gwascentralrs36210420
openSNPrs36210420
23andMers36210420
23andMe allrs36210420
SNP Nexus

SNPshotrs36210420
SNPdbers36210420
MSV3drs36210420
GWAS Ctlgrs36210420
Max Magnitude0


ClinVar
Risk rs36210420(C;C)
Alt rs36210420(C;C)
Reference rs36210420(A;A)
Significance Pathogenic
Disease Torsades de pointes not specified Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Torsades de pointes not specified Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38651288T>G
CLNSRC ClinVar
CLNACC RCV000058854.2, RCV000182950.2, RCV000227263.1,