rs757532106
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs757532106(A;A) |
Make rs757532106(A;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 3 |
Position | 38550500 |
Gene | SCN5A |
is a | snp |
is | mentioned by |
dbSNP | rs757532106 |
dbSNP (classic) | rs757532106 |
ClinGen | rs757532106 |
ebi | rs757532106 |
HLI | rs757532106 |
Exac | rs757532106 |
Gnomad | rs757532106 |
Varsome | rs757532106 |
LitVar | rs757532106 |
Map | rs757532106 |
PheGenI | rs757532106 |
Biobank | rs757532106 |
1000 genomes | rs757532106 |
hgdp | rs757532106 |
ensembl | rs757532106 |
geneview | rs757532106 |
scholar | rs757532106 |
rs757532106 | |
pharmgkb | rs757532106 |
gwascentral | rs757532106 |
openSNP | rs757532106 |
23andMe | rs757532106 |
SNPshot | rs757532106 |
SNPdbe | rs757532106 |
MSV3d | rs757532106 |
GWAS Ctlg | rs757532106 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs757532106(A;A) |
Alt | rs757532106(A;A) |
Reference | Rs757532106(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | SCN5A |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000003.11:g.38591991G>A |
CLNSRC | |
CLNACC | RCV000183137.5, |