rs751931568
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs751931568(A;A) |
Make rs751931568(A;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 21 |
Position | 34370687 |
Gene | KCNE2, LOC105372791 |
is a | snp |
is | mentioned by |
dbSNP | rs751931568 |
dbSNP (classic) | rs751931568 |
ClinGen | rs751931568 |
ebi | rs751931568 |
HLI | rs751931568 |
Exac | rs751931568 |
Gnomad | rs751931568 |
Varsome | rs751931568 |
LitVar | rs751931568 |
Map | rs751931568 |
PheGenI | rs751931568 |
Biobank | rs751931568 |
1000 genomes | rs751931568 |
hgdp | rs751931568 |
ensembl | rs751931568 |
geneview | rs751931568 |
scholar | rs751931568 |
rs751931568 | |
pharmgkb | rs751931568 |
gwascentral | rs751931568 |
openSNP | rs751931568 |
23andMe | rs751931568 |
SNPshot | rs751931568 |
SNPdbe | rs751931568 |
MSV3d | rs751931568 |
GWAS Ctlg | rs751931568 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs751931568(A;A) |
Alt | rs751931568(A;A) |
Reference | Rs751931568(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | KCNE2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000021.8:g.35742986G>A |
CLNSRC | |
CLNACC | RCV000171348.1, |