rs6022990
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs6022990(A;G) |
Make rs6022990(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 20 |
Position | 54158993 |
Gene | CYP24A1 |
is a | snp |
is | mentioned by |
dbSNP | rs6022990 |
dbSNP (classic) | rs6022990 |
ClinGen | rs6022990 |
ebi | rs6022990 |
HLI | rs6022990 |
Exac | rs6022990 |
Gnomad | rs6022990 |
Varsome | rs6022990 |
LitVar | rs6022990 |
Map | rs6022990 |
PheGenI | rs6022990 |
Biobank | rs6022990 |
1000 genomes | rs6022990 |
hgdp | rs6022990 |
ensembl | rs6022990 |
geneview | rs6022990 |
scholar | rs6022990 |
rs6022990 | |
pharmgkb | rs6022990 |
gwascentral | rs6022990 |
openSNP | rs6022990 |
23andMe | rs6022990 |
SNPshot | rs6022990 |
SNPdbe | rs6022990 |
MSV3d | rs6022990 |
GWAS Ctlg | rs6022990 |
GMAF | 0.02388 |
Max Magnitude | 0 |
[PMID 24562971] Genetic variation in vitamin D-related genes and risk of colorectal cancer in African Americans
ClinVar | |
---|---|
Risk | rs6022990(G;G) |
Alt | rs6022990(G;G) |
Reference | Rs6022990(A;A) |
Significance | Probable-non-pathogenic |
Disease | Infantile hypercalcemia |
Variation | info |
Gene | CYP24A1 |
CLNDBN | Infantile hypercalcemia |
Reversed | 0 |
HGVS | NC_000020.10:g.52775532A>G |
CLNSRC | |
CLNACC | RCV000372646.1, |