rs745973997
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs745973997(A;A) |
Make rs745973997(A;G) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 9 |
Position | 2646435 |
Gene | VLDLR |
is a | snp |
is | mentioned by |
dbSNP | rs745973997 |
dbSNP (classic) | rs745973997 |
ClinGen | rs745973997 |
ebi | rs745973997 |
HLI | rs745973997 |
Exac | rs745973997 |
Gnomad | rs745973997 |
Varsome | rs745973997 |
LitVar | rs745973997 |
Map | rs745973997 |
PheGenI | rs745973997 |
Biobank | rs745973997 |
1000 genomes | rs745973997 |
hgdp | rs745973997 |
ensembl | rs745973997 |
geneview | rs745973997 |
scholar | rs745973997 |
rs745973997 | |
pharmgkb | rs745973997 |
gwascentral | rs745973997 |
openSNP | rs745973997 |
23andMe | rs745973997 |
SNPshot | rs745973997 |
SNPdbe | rs745973997 |
MSV3d | rs745973997 |
GWAS Ctlg | rs745973997 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs745973997(A;A) |
Alt | rs745973997(A;A) |
Reference | Rs745973997(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | VLDLR |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000009.11:g.2646435G>A |
CLNSRC | |
CLNACC | RCV000255297.1, |