rs368507376
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs368507376(A;A) |
Make rs368507376(A;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 11 |
Position | 2587583 |
Gene | KCNQ1 |
is a | snp |
is | mentioned by |
dbSNP | rs368507376 |
dbSNP (classic) | rs368507376 |
ClinGen | rs368507376 |
ebi | rs368507376 |
HLI | rs368507376 |
Exac | rs368507376 |
Gnomad | rs368507376 |
Varsome | rs368507376 |
LitVar | rs368507376 |
Map | rs368507376 |
PheGenI | rs368507376 |
Biobank | rs368507376 |
1000 genomes | rs368507376 |
hgdp | rs368507376 |
ensembl | rs368507376 |
geneview | rs368507376 |
scholar | rs368507376 |
rs368507376 | |
pharmgkb | rs368507376 |
gwascentral | rs368507376 |
openSNP | rs368507376 |
23andMe | rs368507376 |
SNPshot | rs368507376 |
SNPdbe | rs368507376 |
MSV3d | rs368507376 |
GWAS Ctlg | rs368507376 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs368507376(A;A) |
Alt | rs368507376(A;A) |
Reference | Rs368507376(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | KCNQ1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000011.9:g.2608813G>A |
CLNSRC | |
CLNACC | RCV000182180.1, |