rs4647707
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs4647707(A;A) |
Make rs4647707(A;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 11 |
Position | 47215017 |
Gene | DDB2 |
is a | snp |
is | mentioned by |
dbSNP | rs4647707 |
dbSNP (classic) | rs4647707 |
ClinGen | rs4647707 |
ebi | rs4647707 |
HLI | rs4647707 |
Exac | rs4647707 |
Gnomad | rs4647707 |
Varsome | rs4647707 |
LitVar | rs4647707 |
Map | rs4647707 |
PheGenI | rs4647707 |
Biobank | rs4647707 |
1000 genomes | rs4647707 |
hgdp | rs4647707 |
ensembl | rs4647707 |
geneview | rs4647707 |
scholar | rs4647707 |
rs4647707 | |
pharmgkb | rs4647707 |
gwascentral | rs4647707 |
openSNP | rs4647707 |
23andMe | rs4647707 |
SNPshot | rs4647707 |
SNPdbe | rs4647707 |
MSV3d | rs4647707 |
GWAS Ctlg | rs4647707 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 26650177] Genetic variations in vitamin D-related pathways and breast cancer risk in African American women in the AMBER Consortium.
ClinVar | |
---|---|
Risk | rs4647707(A;A) |
Alt | rs4647707(A;A) |
Reference | Rs4647707(G;G) |
Significance | Non-pathogenic |
Disease | Xeroderma pigmentosum |
Variation | info |
Gene | DDB2 |
CLNDBN | Xeroderma pigmentosum |
Reversed | 0 |
HGVS | NC_000011.9:g.47236568G>A |
CLNSRC | |
CLNACC | RCV000402377.1, |