rs767086146
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(CT;CT) | 0 | common in clinvar |
Make rs767086146(-;-) |
Make rs767086146(-;CT) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 15 |
Position | 84646300 |
Gene | WDR73 |
is a | snp |
is | mentioned by |
dbSNP | rs767086146 |
dbSNP (classic) | rs767086146 |
ClinGen | rs767086146 |
ebi | rs767086146 |
HLI | rs767086146 |
Exac | rs767086146 |
Gnomad | rs767086146 |
Varsome | rs767086146 |
LitVar | rs767086146 |
Map | rs767086146 |
PheGenI | rs767086146 |
Biobank | rs767086146 |
1000 genomes | rs767086146 |
hgdp | rs767086146 |
ensembl | rs767086146 |
geneview | rs767086146 |
scholar | rs767086146 |
rs767086146 | |
pharmgkb | rs767086146 |
gwascentral | rs767086146 |
openSNP | rs767086146 |
23andMe | rs767086146 |
SNPshot | rs767086146 |
SNPdbe | rs767086146 |
MSV3d | rs767086146 |
GWAS Ctlg | rs767086146 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs767086146(-;-) |
Alt | rs767086146(-;-) |
Reference | Rs767086146(CT;CT) |
Significance | Pathogenic |
Disease | Galloway-Mowat syndrome |
Variation | info |
Gene | WDR73 |
CLNDBN | Galloway-Mowat syndrome |
Reversed | 0 |
HGVS | NC_000015.9:g.85189531_85189532delCT |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000190489.2, |