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rs1060501114

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060501114(A;A)
Make rs1060501114(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position38585842
GeneSCN5A
is asnp
is mentioned by
dbSNPrs1060501114
dbSNP (old)rs1060501114
ClinGenrs1060501114
ebirs1060501114
HLIrs1060501114
Exacrs1060501114
Gnomadrs1060501114
Varsomers1060501114
LitVarrs1060501114
Maprs1060501114
PheGenIrs1060501114
Biobankrs1060501114
1000 genomesrs1060501114
hgdprs1060501114
ensemblrs1060501114
gopubmedrs1060501114
geneviewrs1060501114
scholarrs1060501114
googlers1060501114
pharmgkbrs1060501114
gwascentralrs1060501114
openSNPrs1060501114
23andMers1060501114
23andMe allrs1060501114
SNPshotrs1060501114
SNPdbers1060501114
MSV3drs1060501114
GWAS Ctlgrs1060501114
Max Magnitude0
ClinVar
Risk rs1060501114(A;A)
Alt rs1060501114(A;A)
Reference Rs1060501114(G;G)
Significance Pathogenic
Disease Brugada syndrome
Variation info
Gene SCN5A
CLNDBN Brugada syndrome
Reversed 1
HGVS NC_000003.11:g.38627333C>T
CLNSRC
CLNACC RCV000470092.1,