rs537423012
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs537423012(C;T) |
Make rs537423012(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 3 |
Position | 38562452 |
Gene | SCN5A |
is a | snp |
is | mentioned by |
dbSNP | rs537423012 |
dbSNP (classic) | rs537423012 |
ClinGen | rs537423012 |
ebi | rs537423012 |
HLI | rs537423012 |
Exac | rs537423012 |
Gnomad | rs537423012 |
Varsome | rs537423012 |
LitVar | rs537423012 |
Map | rs537423012 |
PheGenI | rs537423012 |
Biobank | rs537423012 |
1000 genomes | rs537423012 |
hgdp | rs537423012 |
ensembl | rs537423012 |
geneview | rs537423012 |
scholar | rs537423012 |
rs537423012 | |
pharmgkb | rs537423012 |
gwascentral | rs537423012 |
openSNP | rs537423012 |
23andMe | rs537423012 |
SNPshot | rs537423012 |
SNPdbe | rs537423012 |
MSV3d | rs537423012 |
GWAS Ctlg | rs537423012 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs537423012(T;T) |
Alt | rs537423012(T;T) |
Reference | Rs537423012(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | SCN5A |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000003.11:g.38603943C>T |
CLNSRC | |
CLNACC | RCV000183051.2, |