rs191009474
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs191009474(A;A) |
Make rs191009474(A;C) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 3 |
Position | 38606790 |
Gene | SCN5A |
is a | snp |
is | mentioned by |
dbSNP | rs191009474 |
dbSNP (classic) | rs191009474 |
ClinGen | rs191009474 |
ebi | rs191009474 |
HLI | rs191009474 |
Exac | rs191009474 |
Gnomad | rs191009474 |
Varsome | rs191009474 |
LitVar | rs191009474 |
Map | rs191009474 |
PheGenI | rs191009474 |
Biobank | rs191009474 |
1000 genomes | rs191009474 |
hgdp | rs191009474 |
ensembl | rs191009474 |
geneview | rs191009474 |
scholar | rs191009474 |
rs191009474 | |
pharmgkb | rs191009474 |
gwascentral | rs191009474 |
openSNP | rs191009474 |
23andMe | rs191009474 |
SNPshot | rs191009474 |
SNPdbe | rs191009474 |
MSV3d | rs191009474 |
GWAS Ctlg | rs191009474 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs191009474(A;A) rs191009474(T;T) |
Alt | rs191009474(A;A) rs191009474(T;T) |
Reference | Rs191009474(C;C) |
Significance | Untested |
Disease | Congenital long QT syndrome |
Variation | info |
Gene | SCN5A |
CLNDBN | Congenital long QT syndrome |
Reversed | 0 |
HGVS | NC_000003.11:g.38648281C>T |
CLNSRC | ClinVar |
CLNACC | RCV000058382.3, |