rs145961131
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs145961131(A;A) |
Make rs145961131(A;G) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 1 |
Position | 94062608 |
Gene | ABCA4 |
is a | snp |
is | mentioned by |
dbSNP | rs145961131 |
dbSNP (classic) | rs145961131 |
ClinGen | rs145961131 |
ebi | rs145961131 |
HLI | rs145961131 |
Exac | rs145961131 |
Gnomad | rs145961131 |
Varsome | rs145961131 |
LitVar | rs145961131 |
Map | rs145961131 |
PheGenI | rs145961131 |
Biobank | rs145961131 |
1000 genomes | rs145961131 |
hgdp | rs145961131 |
ensembl | rs145961131 |
geneview | rs145961131 |
scholar | rs145961131 |
rs145961131 | |
pharmgkb | rs145961131 |
gwascentral | rs145961131 |
openSNP | rs145961131 |
23andMe | rs145961131 |
SNPshot | rs145961131 |
SNPdbe | rs145961131 |
MSV3d | rs145961131 |
GWAS Ctlg | rs145961131 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs145961131(A;A) |
Alt | rs145961131(A;A) |
Reference | Rs145961131(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | ABCA4 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000001.10:g.94528164G>A |
CLNSRC | |
CLNACC | RCV000256006.1, |