rs754099015
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs754099015(A;A) |
Make rs754099015(A;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 15 |
Position | 84643568 |
Gene | WDR73 |
is a | snp |
is | mentioned by |
dbSNP | rs754099015 |
dbSNP (classic) | rs754099015 |
ClinGen | rs754099015 |
ebi | rs754099015 |
HLI | rs754099015 |
Exac | rs754099015 |
Gnomad | rs754099015 |
Varsome | rs754099015 |
LitVar | rs754099015 |
Map | rs754099015 |
PheGenI | rs754099015 |
Biobank | rs754099015 |
1000 genomes | rs754099015 |
hgdp | rs754099015 |
ensembl | rs754099015 |
geneview | rs754099015 |
scholar | rs754099015 |
rs754099015 | |
pharmgkb | rs754099015 |
gwascentral | rs754099015 |
openSNP | rs754099015 |
23andMe | rs754099015 |
SNPshot | rs754099015 |
SNPdbe | rs754099015 |
MSV3d | rs754099015 |
GWAS Ctlg | rs754099015 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs754099015(A;A) |
Alt | rs754099015(A;A) |
Reference | Rs754099015(G;G) |
Significance | Pathogenic |
Disease | Galloway-Mowat syndrome |
Variation | info |
Gene | WDR73 |
CLNDBN | Galloway-Mowat syndrome |
Reversed | 0 |
HGVS | NC_000015.9:g.85186799G>A |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000190490.3, |