rs121918561
From SNPedia
Merged into | rs61755777 |
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(GCT;GCT) | 0 | common in clinvar |
(TGC;TGC) | 0 | common/normal |
Make rs121918561(-;-) |
Make rs121918561(-;TGC) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 42721981 |
Gene | PRPH2 |
is a | snp |
is | mentioned by |
dbSNP | rs121918561 |
dbSNP (classic) | rs121918561 |
ClinGen | rs121918561 |
ebi | rs121918561 |
HLI | rs121918561 |
Exac | rs121918561 |
Gnomad | rs121918561 |
Varsome | rs121918561 |
LitVar | rs121918561 |
Map | rs121918561 |
PheGenI | rs121918561 |
Biobank | rs121918561 |
1000 genomes | rs121918561 |
hgdp | rs121918561 |
ensembl | rs121918561 |
geneview | rs121918561 |
scholar | rs121918561 |
rs121918561 | |
pharmgkb | rs121918561 |
gwascentral | rs121918561 |
openSNP | rs121918561 |
23andMe | rs121918561 |
SNPshot | rs121918561 |
SNPdbe | rs121918561 |
MSV3d | rs121918561 |
GWAS Ctlg | rs121918561 |
Status | Merged into rs61755777 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | |
Alt | |
Reference | Rs121918561(GCT;GCT) |
Significance | Pathogenic |
Disease | Retinitis pigmentosa 7 not provided |
Variation | info |
Gene | PRPH2 |
CLNDBN | Retinitis pigmentosa 7 not provided |
Reversed | 1 |
HGVS | NC_000006.11:g.42689715_42689717delAGC |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000014048.24, RCV000084963.1, |