rs794728431
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
(I;I) | 0 | common genotype |
Make rs794728431(-;-) |
Make rs794728431(-;C) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 7 |
Position | 150957405 |
Gene | KCNH2 |
is a | snp |
is | mentioned by |
dbSNP | rs794728431 |
dbSNP (classic) | rs794728431 |
ClinGen | rs794728431 |
ebi | rs794728431 |
HLI | rs794728431 |
Exac | rs794728431 |
Gnomad | rs794728431 |
Varsome | rs794728431 |
LitVar | rs794728431 |
Map | rs794728431 |
PheGenI | rs794728431 |
Biobank | rs794728431 |
1000 genomes | rs794728431 |
hgdp | rs794728431 |
ensembl | rs794728431 |
geneview | rs794728431 |
scholar | rs794728431 |
rs794728431 | |
pharmgkb | rs794728431 |
gwascentral | rs794728431 |
openSNP | rs794728431 |
23andMe | rs794728431 |
SNPshot | rs794728431 |
SNPdbe | rs794728431 |
MSV3d | rs794728431 |
GWAS Ctlg | rs794728431 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs794728431(-;-) |
Alt | rs794728431(-;-) |
Reference | Rs794728431(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | KCNH2 |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000007.13:g.150654493delG |
CLNSRC | |
CLNACC | RCV000181969.1, |