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rs730880207

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880207(A;A)
Make rs730880207(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position38562461
GeneSCN5A
is asnp
is mentioned by
dbSNPrs730880207
ebirs730880207
HLIrs730880207
Exacrs730880207
Varsomers730880207
Maprs730880207
PheGenIrs730880207
hapmaprs730880207
1000 genomesrs730880207
hgdprs730880207
ensemblrs730880207
gopubmedrs730880207
geneviewrs730880207
scholarrs730880207
googlers730880207
pharmgkbrs730880207
gwascentralrs730880207
openSNPrs730880207
23andMers730880207
23andMe allrs730880207
SNP Nexus

SNPshotrs730880207
SNPdbers730880207
MSV3drs730880207
GWAS Ctlgrs730880207
Max Magnitude0
ClinVar
Risk rs730880207(A;A)
Alt rs730880207(A;A)
Reference rs730880207(G;G)
Significance Probable-Pathogenic
Disease Brugada syndrome not provided
Variation info
Gene SCN5A
CLNDBN Brugada syndrome not provided
Reversed 1
HGVS NC_000003.11:g.38603952C>T
CLNSRC
CLNACC RCV000157489.1, RCV000183050.2,