rs751386429
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs751386429(A;A) |
Make rs751386429(A;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 4 |
Position | 39253193 |
Gene | WDR19 |
is a | snp |
is | mentioned by |
dbSNP | rs751386429 |
dbSNP (classic) | rs751386429 |
ClinGen | rs751386429 |
ebi | rs751386429 |
HLI | rs751386429 |
Exac | rs751386429 |
Gnomad | rs751386429 |
Varsome | rs751386429 |
LitVar | rs751386429 |
Map | rs751386429 |
PheGenI | rs751386429 |
Biobank | rs751386429 |
1000 genomes | rs751386429 |
hgdp | rs751386429 |
ensembl | rs751386429 |
geneview | rs751386429 |
scholar | rs751386429 |
rs751386429 | |
pharmgkb | rs751386429 |
gwascentral | rs751386429 |
openSNP | rs751386429 |
23andMe | rs751386429 |
SNPshot | rs751386429 |
SNPdbe | rs751386429 |
MSV3d | rs751386429 |
GWAS Ctlg | rs751386429 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs751386429(A;A) rs751386429(T;T) |
Alt | rs751386429(A;A) rs751386429(T;T) |
Reference | Rs751386429(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | WDR19 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000004.11:g.39254813G>T |
CLNSRC | |
CLNACC | RCV000171376.1, |