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rs45627438

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs45627438(A;A)
Make rs45627438(A;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38604025
GeneSCN5A
is asnp
is mentioned by
dbSNPrs45627438
ebirs45627438
HLIrs45627438
Exacrs45627438
Varsomers45627438
Maprs45627438
PheGenIrs45627438
hapmaprs45627438
1000 genomesrs45627438
hgdprs45627438
ensemblrs45627438
gopubmedrs45627438
geneviewrs45627438
scholarrs45627438
googlers45627438
pharmgkbrs45627438
gwascentralrs45627438
openSNPrs45627438
23andMers45627438
23andMe allrs45627438
SNP Nexus

SNPshotrs45627438
SNPdbers45627438
MSV3drs45627438
GWAS Ctlgrs45627438
Max Magnitude0
ClinVar
Risk rs45627438(A;A)
Alt rs45627438(A;A)
Reference rs45627438(G;G)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38645516C>T
CLNSRC ClinVar
CLNACC RCV000058431.2,