rs202033121
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs202033121(A;A) |
Make rs202033121(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 10 |
Position | 53938872 |
Gene | PCDH15 |
is a | snp |
is | mentioned by |
dbSNP | rs202033121 |
dbSNP (classic) | rs202033121 |
ClinGen | rs202033121 |
ebi | rs202033121 |
HLI | rs202033121 |
Exac | rs202033121 |
Gnomad | rs202033121 |
Varsome | rs202033121 |
LitVar | rs202033121 |
Map | rs202033121 |
PheGenI | rs202033121 |
Biobank | rs202033121 |
1000 genomes | rs202033121 |
hgdp | rs202033121 |
ensembl | rs202033121 |
geneview | rs202033121 |
scholar | rs202033121 |
rs202033121 | |
pharmgkb | rs202033121 |
gwascentral | rs202033121 |
openSNP | rs202033121 |
23andMe | rs202033121 |
SNPshot | rs202033121 |
SNPdbe | rs202033121 |
MSV3d | rs202033121 |
GWAS Ctlg | rs202033121 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs202033121(A;A) |
Alt | rs202033121(A;A) |
Reference | Rs202033121(G;G) |
Significance | Other |
Disease | Usher syndrome |
Variation | info |
Gene | PCDH15 |
CLNDBN | Usher syndrome, type 1F |
Reversed | 0 |
HGVS | NC_000010.10:g.55698632G>A |
CLNSRC | ClinVar |
CLNACC | RCV000039723.4, |