rs750013499
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs750013499(A;G) |
Make rs750013499(G;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 3 |
Position | 38551345 |
Gene | SCN5A |
is a | snp |
is | mentioned by |
dbSNP | rs750013499 |
dbSNP (classic) | rs750013499 |
ClinGen | rs750013499 |
ebi | rs750013499 |
HLI | rs750013499 |
Exac | rs750013499 |
Gnomad | rs750013499 |
Varsome | rs750013499 |
LitVar | rs750013499 |
Map | rs750013499 |
PheGenI | rs750013499 |
Biobank | rs750013499 |
1000 genomes | rs750013499 |
hgdp | rs750013499 |
ensembl | rs750013499 |
geneview | rs750013499 |
scholar | rs750013499 |
rs750013499 | |
pharmgkb | rs750013499 |
gwascentral | rs750013499 |
openSNP | rs750013499 |
23andMe | rs750013499 |
SNPshot | rs750013499 |
SNPdbe | rs750013499 |
MSV3d | rs750013499 |
GWAS Ctlg | rs750013499 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs750013499(G;G) |
Alt | rs750013499(G;G) |
Reference | Rs750013499(A;A) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | SCN5A |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000003.11:g.38592836A>G |
CLNSRC | |
CLNACC | RCV000183097.1, |