rs2856585
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs2856585(A;A) |
Make rs2856585(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 16169806 |
Gene | ABCC6 |
is a | snp |
is | mentioned by |
dbSNP | rs2856585 |
dbSNP (classic) | rs2856585 |
ClinGen | rs2856585 |
ebi | rs2856585 |
HLI | rs2856585 |
Exac | rs2856585 |
Gnomad | rs2856585 |
Varsome | rs2856585 |
LitVar | rs2856585 |
Map | rs2856585 |
PheGenI | rs2856585 |
Biobank | rs2856585 |
1000 genomes | rs2856585 |
hgdp | rs2856585 |
ensembl | rs2856585 |
geneview | rs2856585 |
scholar | rs2856585 |
rs2856585 | |
pharmgkb | rs2856585 |
gwascentral | rs2856585 |
openSNP | rs2856585 |
23andMe | rs2856585 |
SNPshot | rs2856585 |
SNPdbe | rs2856585 |
MSV3d | rs2856585 |
GWAS Ctlg | rs2856585 |
GMAF | 0.1364 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
ClinVar | |
---|---|
Risk | rs2856585(A;A) |
Alt | rs2856585(A;A) |
Reference | Rs2856585(G;G) |
Significance | Untested |
Disease | |
Variation | info |
Gene | ABCC6 |
CLNDBN | |
Reversed | 0 |
HGVS | NC_000016.9:g.16263663G>A |
CLNSRC | |
CLNACC |