rs9940825
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs9940825(C;T) |
Make rs9940825(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 16198114 |
Gene | ABCC6 |
is a | snp |
is | mentioned by |
dbSNP | rs9940825 |
dbSNP (classic) | rs9940825 |
ClinGen | rs9940825 |
ebi | rs9940825 |
HLI | rs9940825 |
Exac | rs9940825 |
Gnomad | rs9940825 |
Varsome | rs9940825 |
LitVar | rs9940825 |
Map | rs9940825 |
PheGenI | rs9940825 |
Biobank | rs9940825 |
1000 genomes | rs9940825 |
hgdp | rs9940825 |
ensembl | rs9940825 |
geneview | rs9940825 |
scholar | rs9940825 |
rs9940825 | |
pharmgkb | rs9940825 |
gwascentral | rs9940825 |
openSNP | rs9940825 |
23andMe | rs9940825 |
SNPshot | rs9940825 |
SNPdbe | rs9940825 |
MSV3d | rs9940825 |
GWAS Ctlg | rs9940825 |
GMAF | 0.2383 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs9940825(T;T) |
Alt | rs9940825(T;T) |
Reference | Rs9940825(C;C) |
Significance | Untested |
Disease | |
Variation | info |
Gene | ABCC6 |
CLNDBN | |
Reversed | 0 |
HGVS | NC_000016.9:g.16291971C>T |
CLNSRC | |
CLNACC |