rs57499803
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs57499803(C;T) |
Make rs57499803(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 16154936 |
Gene | ABCC6 |
is a | snp |
is | mentioned by |
dbSNP | rs57499803 |
dbSNP (classic) | rs57499803 |
ClinGen | rs57499803 |
ebi | rs57499803 |
HLI | rs57499803 |
Exac | rs57499803 |
Gnomad | rs57499803 |
Varsome | rs57499803 |
LitVar | rs57499803 |
Map | rs57499803 |
PheGenI | rs57499803 |
Biobank | rs57499803 |
1000 genomes | rs57499803 |
hgdp | rs57499803 |
ensembl | rs57499803 |
geneview | rs57499803 |
scholar | rs57499803 |
rs57499803 | |
pharmgkb | rs57499803 |
gwascentral | rs57499803 |
openSNP | rs57499803 |
23andMe | rs57499803 |
SNPshot | rs57499803 |
SNPdbe | rs57499803 |
MSV3d | rs57499803 |
GWAS Ctlg | rs57499803 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs57499803(T;T) |
Alt | rs57499803(T;T) |
Reference | Rs57499803(C;C) |
Significance | Untested |
Disease | |
Variation | info |
Gene | ABCC6 |
CLNDBN | |
Reversed | 1 |
HGVS | NC_000016.9:g.16248793G>A |
CLNSRC | |
CLNACC |