rs557957405
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs557957405(A;A) |
Make rs557957405(A;C) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 3 |
Position | 38576768 |
Gene | SCN5A |
is a | snp |
is | mentioned by |
dbSNP | rs557957405 |
dbSNP (classic) | rs557957405 |
ClinGen | rs557957405 |
ebi | rs557957405 |
HLI | rs557957405 |
Exac | rs557957405 |
Gnomad | rs557957405 |
Varsome | rs557957405 |
LitVar | rs557957405 |
Map | rs557957405 |
PheGenI | rs557957405 |
Biobank | rs557957405 |
1000 genomes | rs557957405 |
hgdp | rs557957405 |
ensembl | rs557957405 |
geneview | rs557957405 |
scholar | rs557957405 |
rs557957405 | |
pharmgkb | rs557957405 |
gwascentral | rs557957405 |
openSNP | rs557957405 |
23andMe | rs557957405 |
SNPshot | rs557957405 |
SNPdbe | rs557957405 |
MSV3d | rs557957405 |
GWAS Ctlg | rs557957405 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs557957405(A;A) |
Alt | rs557957405(A;A) |
Reference | Rs557957405(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | SCN5A |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000003.11:g.38618259C>A |
CLNSRC | |
CLNACC | RCV000183035.1, |