rs77775126
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs77775126(C;T) |
Make rs77775126(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 8 |
Position | 54625000 |
Gene | RP1 |
is a | snp |
is | mentioned by |
dbSNP | rs77775126 |
dbSNP (classic) | rs77775126 |
ClinGen | rs77775126 |
ebi | rs77775126 |
HLI | rs77775126 |
Exac | rs77775126 |
Gnomad | rs77775126 |
Varsome | rs77775126 |
LitVar | rs77775126 |
Map | rs77775126 |
PheGenI | rs77775126 |
Biobank | rs77775126 |
1000 genomes | rs77775126 |
hgdp | rs77775126 |
ensembl | rs77775126 |
geneview | rs77775126 |
scholar | rs77775126 |
rs77775126 | |
pharmgkb | rs77775126 |
gwascentral | rs77775126 |
openSNP | rs77775126 |
23andMe | rs77775126 |
SNPshot | rs77775126 |
SNPdbe | rs77775126 |
MSV3d | rs77775126 |
GWAS Ctlg | rs77775126 |
GMAF | 0.008264 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs77775126(T;T) |
Alt | rs77775126(T;T) |
Reference | Rs77775126(C;C) |
Significance | Other |
Disease | Retinitis pigmentosa 1 not specified Retinitis Pigmentosa |
Variation | info |
Gene | RP1 |
CLNDBN | Retinitis pigmentosa 1 not specified Retinitis Pigmentosa, Dominant |
Reversed | 0 |
HGVS | NC_000008.10:g.55537560C>T |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000006334.3, RCV000178267.2, RCV000270795.1, |