rs367891946
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs367891946(C;G) |
Make rs367891946(G;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 15 |
Position | 40418127 |
Gene | IVD |
is a | snp |
is | mentioned by |
dbSNP | rs367891946 |
dbSNP (classic) | rs367891946 |
ClinGen | rs367891946 |
ebi | rs367891946 |
HLI | rs367891946 |
Exac | rs367891946 |
Gnomad | rs367891946 |
Varsome | rs367891946 |
LitVar | rs367891946 |
Map | rs367891946 |
PheGenI | rs367891946 |
Biobank | rs367891946 |
1000 genomes | rs367891946 |
hgdp | rs367891946 |
ensembl | rs367891946 |
geneview | rs367891946 |
scholar | rs367891946 |
rs367891946 | |
pharmgkb | rs367891946 |
gwascentral | rs367891946 |
openSNP | rs367891946 |
23andMe | rs367891946 |
SNPshot | rs367891946 |
SNPdbe | rs367891946 |
MSV3d | rs367891946 |
GWAS Ctlg | rs367891946 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs367891946(G;G) |
Alt | rs367891946(G;G) |
Reference | Rs367891946(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | IVD |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000015.9:g.40710326C>G |
CLNSRC | |
CLNACC | RCV000185977.1, |