rs1064793935
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Chromosome | 22 |
Position | 26616149 |
Gene | CRYBA4, CRYBB1 |
is a | snp |
is | mentioned by |
dbSNP | rs1064793935 |
dbSNP (classic) | rs1064793935 |
ClinGen | rs1064793935 |
ebi | rs1064793935 |
HLI | rs1064793935 |
Exac | rs1064793935 |
Gnomad | rs1064793935 |
Varsome | rs1064793935 |
LitVar | rs1064793935 |
Map | rs1064793935 |
PheGenI | rs1064793935 |
Biobank | rs1064793935 |
1000 genomes | rs1064793935 |
hgdp | rs1064793935 |
ensembl | rs1064793935 |
geneview | rs1064793935 |
scholar | rs1064793935 |
rs1064793935 | |
pharmgkb | rs1064793935 |
gwascentral | rs1064793935 |
openSNP | rs1064793935 |
23andMe | rs1064793935 |
SNPshot | rs1064793935 |
SNPdbe | rs1064793935 |
MSV3d | rs1064793935 |
GWAS Ctlg | rs1064793935 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1064793935(-;-) |
Alt | rs1064793935(-;-) |
Reference | Rs1064793935(G;G) |
Significance | Pathogenic |
Disease | Cataract not provided |
Variation | info |
Gene | CRYBB1 |
CLNDBN | Cataract, congenital nuclear, autosomal recessive 3 not provided |
Reversed | 1 |
HGVS | NC_000022.10:g.27012113delC |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000009225.5, RCV000486232.1, |