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rs137854620

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137854620(A;A)
Make rs137854620(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position38557268
GeneSCN5A
is asnp
is mentioned by
dbSNPrs137854620
ebirs137854620
HLIrs137854620
Exacrs137854620
Varsomers137854620
Maprs137854620
PheGenIrs137854620
hapmaprs137854620
1000 genomesrs137854620
hgdprs137854620
ensemblrs137854620
gopubmedrs137854620
geneviewrs137854620
scholarrs137854620
googlers137854620
pharmgkbrs137854620
gwascentralrs137854620
openSNPrs137854620
23andMers137854620
23andMe allrs137854620
SNP Nexus

SNPshotrs137854620
SNPdbers137854620
MSV3drs137854620
GWAS Ctlgrs137854620
Max Magnitude0
OMIM600163
Desc
Variant0036
Relatedalso
ClinVar
Risk rs137854620(A;A)
Alt rs137854620(A;A)
Reference rs137854620(G;G)
Significance Pathogenic
Disease Brugada syndrome 1
Variation info
Gene SCN5A
CLNDBN Brugada syndrome 1
Reversed 1
HGVS NC_000003.11:g.38598759C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000010006.4,