rs794728402
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs794728402(G;T) |
Make rs794728402(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 7 |
Position | 150947473 |
Gene | KCNH2 |
is a | snp |
is | mentioned by |
dbSNP | rs794728402 |
dbSNP (classic) | rs794728402 |
ClinGen | rs794728402 |
ebi | rs794728402 |
HLI | rs794728402 |
Exac | rs794728402 |
Gnomad | rs794728402 |
Varsome | rs794728402 |
LitVar | rs794728402 |
Map | rs794728402 |
PheGenI | rs794728402 |
Biobank | rs794728402 |
1000 genomes | rs794728402 |
hgdp | rs794728402 |
ensembl | rs794728402 |
geneview | rs794728402 |
scholar | rs794728402 |
rs794728402 | |
pharmgkb | rs794728402 |
gwascentral | rs794728402 |
openSNP | rs794728402 |
23andMe | rs794728402 |
SNPshot | rs794728402 |
SNPdbe | rs794728402 |
MSV3d | rs794728402 |
GWAS Ctlg | rs794728402 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs794728402(A;A) rs794728402(T;T) |
Alt | rs794728402(A;A) rs794728402(T;T) |
Reference | Rs794728402(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided not specified |
Variation | info |
Gene | KCNH2 |
CLNDBN | not provided not specified |
Reversed | 1 |
HGVS | NC_000007.13:g.150644561C>A; NC_000007.13:g.150644561C>T |
CLNSRC | |
CLNACC | RCV000181906.1, RCV000413178.1, |