rs751787337
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs751787337(C;T) |
Make rs751787337(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 3 |
Position | 38555686 |
Gene | SCN5A |
is a | snp |
is | mentioned by |
dbSNP | rs751787337 |
dbSNP (classic) | rs751787337 |
ClinGen | rs751787337 |
ebi | rs751787337 |
HLI | rs751787337 |
Exac | rs751787337 |
Gnomad | rs751787337 |
Varsome | rs751787337 |
LitVar | rs751787337 |
Map | rs751787337 |
PheGenI | rs751787337 |
Biobank | rs751787337 |
1000 genomes | rs751787337 |
hgdp | rs751787337 |
ensembl | rs751787337 |
geneview | rs751787337 |
scholar | rs751787337 |
rs751787337 | |
pharmgkb | rs751787337 |
gwascentral | rs751787337 |
openSNP | rs751787337 |
23andMe | rs751787337 |
SNPshot | rs751787337 |
SNPdbe | rs751787337 |
MSV3d | rs751787337 |
GWAS Ctlg | rs751787337 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs751787337(A;A) rs751787337(T;T) |
Alt | rs751787337(A;A) rs751787337(T;T) |
Reference | Rs751787337(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | SCN5A |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000003.11:g.38597177C>A |
CLNSRC | |
CLNACC | RCV000183080.1, |