rs878853266
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs878853266(-;A) |
Make rs878853266(A;A) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 3 |
Position | 3148101 |
Gene | CRBN, TRNT1 |
is a | snp |
is | mentioned by |
dbSNP | rs878853266 |
dbSNP (classic) | rs878853266 |
ClinGen | rs878853266 |
ebi | rs878853266 |
HLI | rs878853266 |
Exac | rs878853266 |
Gnomad | rs878853266 |
Varsome | rs878853266 |
LitVar | rs878853266 |
Map | rs878853266 |
PheGenI | rs878853266 |
Biobank | rs878853266 |
1000 genomes | rs878853266 |
hgdp | rs878853266 |
ensembl | rs878853266 |
geneview | rs878853266 |
scholar | rs878853266 |
rs878853266 | |
pharmgkb | rs878853266 |
gwascentral | rs878853266 |
openSNP | rs878853266 |
23andMe | rs878853266 |
SNPshot | rs878853266 |
SNPdbe | rs878853266 |
MSV3d | rs878853266 |
GWAS Ctlg | rs878853266 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs878853266(A;A) |
Alt | rs878853266(A;A) |
Reference | Rs878853266(-;-) |
Significance | Pathogenic |
Disease | Retinitis pigmentosa and erythrocytic microcytosis |
Variation | info |
Gene | TRNT1 |
CLNDBN | Retinitis pigmentosa and erythrocytic microcytosis |
Reversed | 0 |
HGVS | NC_000003.11:g.3189785dupA |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000223673.1, |