rs375548374
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs375548374(A;A) |
Make rs375548374(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 12 |
Position | 88053733 |
Gene | CEP290 |
is a | snp |
is | mentioned by |
dbSNP | rs375548374 |
dbSNP (classic) | rs375548374 |
ClinGen | rs375548374 |
ebi | rs375548374 |
HLI | rs375548374 |
Exac | rs375548374 |
Gnomad | rs375548374 |
Varsome | rs375548374 |
LitVar | rs375548374 |
Map | rs375548374 |
PheGenI | rs375548374 |
Biobank | rs375548374 |
1000 genomes | rs375548374 |
hgdp | rs375548374 |
ensembl | rs375548374 |
geneview | rs375548374 |
scholar | rs375548374 |
rs375548374 | |
pharmgkb | rs375548374 |
gwascentral | rs375548374 |
openSNP | rs375548374 |
23andMe | rs375548374 |
SNPshot | rs375548374 |
SNPdbe | rs375548374 |
MSV3d | rs375548374 |
GWAS Ctlg | rs375548374 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs375548374(A;A) rs375548374(T;T) |
Alt | rs375548374(A;A) rs375548374(T;T) |
Reference | Rs375548374(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | CEP290 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000012.11:g.88447510G>T |
CLNSRC | |
CLNACC | RCV000415801.1, |