rs142223793
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs142223793(A;A) |
Make rs142223793(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 16 |
Position | 16178820 |
Gene | ABCC6 |
is a | snp |
is | mentioned by |
dbSNP | rs142223793 |
dbSNP (classic) | rs142223793 |
ClinGen | rs142223793 |
ebi | rs142223793 |
HLI | rs142223793 |
Exac | rs142223793 |
Gnomad | rs142223793 |
Varsome | rs142223793 |
LitVar | rs142223793 |
Map | rs142223793 |
PheGenI | rs142223793 |
Biobank | rs142223793 |
1000 genomes | rs142223793 |
hgdp | rs142223793 |
ensembl | rs142223793 |
geneview | rs142223793 |
scholar | rs142223793 |
rs142223793 | |
pharmgkb | rs142223793 |
gwascentral | rs142223793 |
openSNP | rs142223793 |
23andMe | rs142223793 |
SNPshot | rs142223793 |
SNPdbe | rs142223793 |
MSV3d | rs142223793 |
GWAS Ctlg | rs142223793 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs142223793(A;A) |
Alt | rs142223793(A;A) |
Reference | Rs142223793(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | ABCC6 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000016.9:g.16272677G>A |
CLNSRC | |
CLNACC | RCV000489677.1, |