rs61744404
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs61744404(C;G) |
Make rs61744404(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 232525489 |
Gene | CHRND, PRSS56 |
is a | snp |
is | mentioned by |
dbSNP | rs61744404 |
dbSNP (classic) | rs61744404 |
ClinGen | rs61744404 |
ebi | rs61744404 |
HLI | rs61744404 |
Exac | rs61744404 |
Gnomad | rs61744404 |
Varsome | rs61744404 |
LitVar | rs61744404 |
Map | rs61744404 |
PheGenI | rs61744404 |
Biobank | rs61744404 |
1000 genomes | rs61744404 |
hgdp | rs61744404 |
ensembl | rs61744404 |
geneview | rs61744404 |
scholar | rs61744404 |
rs61744404 | |
pharmgkb | rs61744404 |
gwascentral | rs61744404 |
openSNP | rs61744404 |
23andMe | rs61744404 |
SNPshot | rs61744404 |
SNPdbe | rs61744404 |
MSV3d | rs61744404 |
GWAS Ctlg | rs61744404 |
GMAF | 0.02342 |
Max Magnitude | 0 |
ClinVar: benign
ClinVar | |
---|---|
Risk | rs61744404(A;A) rs61744404(G;G) |
Alt | rs61744404(A;A) rs61744404(G;G) |
Reference | Rs61744404(C;C) |
Significance | Non-pathogenic |
Disease | Microphthalmia not specified |
Variation | info |
Gene | CHRND PRSS56 |
CLNDBN | Microphthalmia, isolated 6 not specified |
Reversed | 0 |
HGVS | NC_000002.11:g.233390199C>G |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000024074.2, RCV000454640.1, |