rs201855602
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs201855602(A;A) |
Make rs201855602(A;G) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 1 |
Position | 94043470 |
Gene | ABCA4 |
is a | snp |
is | mentioned by |
dbSNP | rs201855602 |
dbSNP (classic) | rs201855602 |
ClinGen | rs201855602 |
ebi | rs201855602 |
HLI | rs201855602 |
Exac | rs201855602 |
Gnomad | rs201855602 |
Varsome | rs201855602 |
LitVar | rs201855602 |
Map | rs201855602 |
PheGenI | rs201855602 |
Biobank | rs201855602 |
1000 genomes | rs201855602 |
hgdp | rs201855602 |
ensembl | rs201855602 |
geneview | rs201855602 |
scholar | rs201855602 |
rs201855602 | |
pharmgkb | rs201855602 |
gwascentral | rs201855602 |
openSNP | rs201855602 |
23andMe | rs201855602 |
SNPshot | rs201855602 |
SNPdbe | rs201855602 |
MSV3d | rs201855602 |
GWAS Ctlg | rs201855602 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs201855602(A;A) |
Alt | rs201855602(A;A) |
Reference | Rs201855602(G;G) |
Significance | Pathogenic |
Disease | Stargardt disease 1 not provided |
Variation | info |
Gene | ABCA4 |
CLNDBN | Stargardt disease 1 not provided |
Reversed | 0 |
HGVS | NC_000001.10:g.94509026G>A |
CLNSRC | |
CLNACC | RCV000406318.1, RCV000412846.1, |