rs372354156
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs372354156(A;T) |
Make rs372354156(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 6 |
Position | 65057696 |
Gene | EYS |
is a | snp |
is | mentioned by |
dbSNP | rs372354156 |
dbSNP (classic) | rs372354156 |
ClinGen | rs372354156 |
ebi | rs372354156 |
HLI | rs372354156 |
Exac | rs372354156 |
Gnomad | rs372354156 |
Varsome | rs372354156 |
LitVar | rs372354156 |
Map | rs372354156 |
PheGenI | rs372354156 |
Biobank | rs372354156 |
1000 genomes | rs372354156 |
hgdp | rs372354156 |
ensembl | rs372354156 |
geneview | rs372354156 |
scholar | rs372354156 |
rs372354156 | |
pharmgkb | rs372354156 |
gwascentral | rs372354156 |
openSNP | rs372354156 |
23andMe | rs372354156 |
SNPshot | rs372354156 |
SNPdbe | rs372354156 |
MSV3d | rs372354156 |
GWAS Ctlg | rs372354156 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs372354156(T;T) |
Alt | rs372354156(T;T) |
Reference | Rs372354156(A;A) |
Significance | Pathogenic |
Disease | Retinitis pigmentosa 25 |
Variation | info |
Gene | EYS |
CLNDBN | Retinitis pigmentosa 25 |
Reversed | 0 |
HGVS | NC_000006.11:g.65767589A>T |
CLNSRC | |
CLNACC | RCV000174505.1, |