rs761117662
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs761117662(C;G) |
Make rs761117662(G;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 3 |
Position | 38606016 |
Gene | SCN5A |
is a | snp |
is | mentioned by |
dbSNP | rs761117662 |
dbSNP (classic) | rs761117662 |
ClinGen | rs761117662 |
ebi | rs761117662 |
HLI | rs761117662 |
Exac | rs761117662 |
Gnomad | rs761117662 |
Varsome | rs761117662 |
LitVar | rs761117662 |
Map | rs761117662 |
PheGenI | rs761117662 |
Biobank | rs761117662 |
1000 genomes | rs761117662 |
hgdp | rs761117662 |
ensembl | rs761117662 |
geneview | rs761117662 |
scholar | rs761117662 |
rs761117662 | |
pharmgkb | rs761117662 |
gwascentral | rs761117662 |
openSNP | rs761117662 |
23andMe | rs761117662 |
SNPshot | rs761117662 |
SNPdbe | rs761117662 |
MSV3d | rs761117662 |
GWAS Ctlg | rs761117662 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs761117662(G;G) rs761117662(T;T) |
Alt | rs761117662(G;G) rs761117662(T;T) |
Reference | Rs761117662(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | SCN5A |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000003.11:g.38647507C>T |
CLNSRC | |
CLNACC | RCV000182966.2, |