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rs1060501136

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060501136(G;T)
Make rs1060501136(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position38609764
GeneSCN5A
is asnp
is mentioned by
dbSNPrs1060501136
dbSNP (old)rs1060501136
ClinGenrs1060501136
ebirs1060501136
HLIrs1060501136
Exacrs1060501136
Gnomadrs1060501136
Varsomers1060501136
Maprs1060501136
PheGenIrs1060501136
Biobankrs1060501136
1000 genomesrs1060501136
hgdprs1060501136
ensemblrs1060501136
gopubmedrs1060501136
geneviewrs1060501136
scholarrs1060501136
googlers1060501136
pharmgkbrs1060501136
gwascentralrs1060501136
openSNPrs1060501136
23andMers1060501136
23andMe allrs1060501136
SNPshotrs1060501136
SNPdbers1060501136
MSV3drs1060501136
GWAS Ctlgrs1060501136
Max Magnitude0
ClinVar
Risk rs1060501136(T;T)
Alt rs1060501136(T;T)
Reference Rs1060501136(G;G)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38651255C>A
CLNSRC
CLNACC RCV000476810.1,