rs763182554
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs763182554(A;C) |
Make rs763182554(C;C) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 2 |
Position | 215011969 |
Gene | ABCA12 |
is a | snp |
is | mentioned by |
dbSNP | rs763182554 |
dbSNP (classic) | rs763182554 |
ClinGen | rs763182554 |
ebi | rs763182554 |
HLI | rs763182554 |
Exac | rs763182554 |
Gnomad | rs763182554 |
Varsome | rs763182554 |
LitVar | rs763182554 |
Map | rs763182554 |
PheGenI | rs763182554 |
Biobank | rs763182554 |
1000 genomes | rs763182554 |
hgdp | rs763182554 |
ensembl | rs763182554 |
geneview | rs763182554 |
scholar | rs763182554 |
rs763182554 | |
pharmgkb | rs763182554 |
gwascentral | rs763182554 |
openSNP | rs763182554 |
23andMe | rs763182554 |
SNPshot | rs763182554 |
SNPdbe | rs763182554 |
MSV3d | rs763182554 |
GWAS Ctlg | rs763182554 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs763182554(C;C) rs763182554(G;G) |
Alt | rs763182554(C;C) rs763182554(G;G) |
Reference | Rs763182554(A;A) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | ABCA12 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000002.11:g.215876693A>C |
CLNSRC | |
CLNACC | RCV000428022.1, |