rs112005636
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs112005636(A;G) |
Make rs112005636(G;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 1 |
Position | 93996107 |
Gene | ABCA4 |
is a | snp |
is | mentioned by |
dbSNP | rs112005636 |
dbSNP (classic) | rs112005636 |
ClinGen | rs112005636 |
ebi | rs112005636 |
HLI | rs112005636 |
Exac | rs112005636 |
Gnomad | rs112005636 |
Varsome | rs112005636 |
LitVar | rs112005636 |
Map | rs112005636 |
PheGenI | rs112005636 |
Biobank | rs112005636 |
1000 genomes | rs112005636 |
hgdp | rs112005636 |
ensembl | rs112005636 |
geneview | rs112005636 |
scholar | rs112005636 |
rs112005636 | |
pharmgkb | rs112005636 |
gwascentral | rs112005636 |
openSNP | rs112005636 |
23andMe | rs112005636 |
SNPshot | rs112005636 |
SNPdbe | rs112005636 |
MSV3d | rs112005636 |
GWAS Ctlg | rs112005636 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs112005636(G;G) rs112005636(T;T) |
Alt | rs112005636(G;G) rs112005636(T;T) |
Reference | Rs112005636(A;A) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | ABCA4 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000001.10:g.94461663A>T |
CLNSRC | |
CLNACC | RCV000487635.1, |