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rs1057518916

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518916(C;T)
Make rs1057518916(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position38606034
GeneSCN5A
is asnp
is mentioned by
dbSNPrs1057518916
dbSNP (old)rs1057518916
ClinGenrs1057518916
ebirs1057518916
HLIrs1057518916
Exacrs1057518916
Gnomadrs1057518916
Varsomers1057518916
Maprs1057518916
PheGenIrs1057518916
Biobankrs1057518916
1000 genomesrs1057518916
hgdprs1057518916
ensemblrs1057518916
gopubmedrs1057518916
geneviewrs1057518916
scholarrs1057518916
googlers1057518916
pharmgkbrs1057518916
gwascentralrs1057518916
openSNPrs1057518916
23andMers1057518916
23andMe allrs1057518916
SNPshotrs1057518916
SNPdbers1057518916
MSV3drs1057518916
GWAS Ctlgrs1057518916
Max Magnitude0
ClinVar
Risk rs1057518916(T;T)
Alt rs1057518916(T;T)
Reference Rs1057518916(C;C)
Significance Probable-Pathogenic
Disease Syncope
Variation info
Gene SCN5A
CLNDBN Syncope
Reversed 1
HGVS NC_000003.11:g.38647525G>A
CLNSRC
CLNACC RCV000415454.1,