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rs1060501142

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060501142(-;-)
Make rs1060501142(-;G)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position38633204
GeneSCN5A
is asnp
is mentioned by
dbSNPrs1060501142
dbSNP (old)rs1060501142
ClinGenrs1060501142
ebirs1060501142
HLIrs1060501142
Exacrs1060501142
Gnomadrs1060501142
Varsomers1060501142
LitVarrs1060501142
Maprs1060501142
PheGenIrs1060501142
Biobankrs1060501142
1000 genomesrs1060501142
hgdprs1060501142
ensemblrs1060501142
gopubmedrs1060501142
geneviewrs1060501142
scholarrs1060501142
googlers1060501142
pharmgkbrs1060501142
gwascentralrs1060501142
openSNPrs1060501142
23andMers1060501142
23andMe allrs1060501142
SNPshotrs1060501142
SNPdbers1060501142
MSV3drs1060501142
GWAS Ctlgrs1060501142
Max Magnitude0
ClinVar
Risk rs1060501142(-;-)
Alt rs1060501142(-;-)
Reference Rs1060501142(G;G)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38674695delC
CLNSRC
CLNACC RCV000456961.1,