rs886041382
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs886041382(C;T) |
Make rs886041382(T;T) |
Chromosome | X |
Position | 49078077 |
Gene | WDR45 |
is a | snp |
is | mentioned by |
dbSNP | rs886041382 |
dbSNP (classic) | rs886041382 |
ClinGen | rs886041382 |
ebi | rs886041382 |
HLI | rs886041382 |
Exac | rs886041382 |
Gnomad | rs886041382 |
Varsome | rs886041382 |
LitVar | rs886041382 |
Map | rs886041382 |
PheGenI | rs886041382 |
Biobank | rs886041382 |
1000 genomes | rs886041382 |
hgdp | rs886041382 |
ensembl | rs886041382 |
geneview | rs886041382 |
scholar | rs886041382 |
rs886041382 | |
pharmgkb | rs886041382 |
gwascentral | rs886041382 |
openSNP | rs886041382 |
23andMe | rs886041382 |
SNPshot | rs886041382 |
SNPdbe | rs886041382 |
MSV3d | rs886041382 |
GWAS Ctlg | rs886041382 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs886041382(T;T) |
Alt | rs886041382(T;T) |
Reference | Rs886041382(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | WDR45 |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000023.10:g.48935736G>A |
CLNSRC | |
CLNACC | RCV000272581.1, |