rs878853379
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs878853379(A;A) |
Make rs878853379(A;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 3 |
Position | 150972611 |
Gene | CLRN1, CLRN1-AS1 |
is a | snp |
is | mentioned by |
dbSNP | rs878853379 |
dbSNP (classic) | rs878853379 |
ClinGen | rs878853379 |
ebi | rs878853379 |
HLI | rs878853379 |
Exac | rs878853379 |
Gnomad | rs878853379 |
Varsome | rs878853379 |
LitVar | rs878853379 |
Map | rs878853379 |
PheGenI | rs878853379 |
Biobank | rs878853379 |
1000 genomes | rs878853379 |
hgdp | rs878853379 |
ensembl | rs878853379 |
geneview | rs878853379 |
scholar | rs878853379 |
rs878853379 | |
pharmgkb | rs878853379 |
gwascentral | rs878853379 |
openSNP | rs878853379 |
23andMe | rs878853379 |
SNPshot | rs878853379 |
SNPdbe | rs878853379 |
MSV3d | rs878853379 |
GWAS Ctlg | rs878853379 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs878853379(A;A) |
Alt | rs878853379(A;A) |
Reference | Rs878853379(G;G) |
Significance | Probable-Pathogenic |
Disease | Retinal dystrophy |
Variation | info |
Gene | CLRN1-AS1 CLRN1 |
CLNDBN | Retinal dystrophy |
Reversed | 1 |
HGVS | NC_000003.11:g.150690398C>T |
CLNSRC | |
CLNACC | RCV000225684.1, |