rs757520757
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs757520757(A;A) |
Make rs757520757(A;G) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 2 |
Position | 215019784 |
Gene | ABCA12 |
is a | snp |
is | mentioned by |
dbSNP | rs757520757 |
dbSNP (classic) | rs757520757 |
ClinGen | rs757520757 |
ebi | rs757520757 |
HLI | rs757520757 |
Exac | rs757520757 |
Gnomad | rs757520757 |
Varsome | rs757520757 |
LitVar | rs757520757 |
Map | rs757520757 |
PheGenI | rs757520757 |
Biobank | rs757520757 |
1000 genomes | rs757520757 |
hgdp | rs757520757 |
ensembl | rs757520757 |
geneview | rs757520757 |
scholar | rs757520757 |
rs757520757 | |
pharmgkb | rs757520757 |
gwascentral | rs757520757 |
openSNP | rs757520757 |
23andMe | rs757520757 |
SNPshot | rs757520757 |
SNPdbe | rs757520757 |
MSV3d | rs757520757 |
GWAS Ctlg | rs757520757 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs757520757(A;A) |
Alt | rs757520757(A;A) |
Reference | Rs757520757(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | ABCA12 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000002.11:g.215884508G>A |
CLNSRC | |
CLNACC | RCV000255533.1, |