rs757091694
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs757091694(C;C) |
Make rs757091694(C;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 19 |
Position | 36067906 |
Gene | WDR62 |
is a | snp |
is | mentioned by |
dbSNP | rs757091694 |
dbSNP (classic) | rs757091694 |
ClinGen | rs757091694 |
ebi | rs757091694 |
HLI | rs757091694 |
Exac | rs757091694 |
Gnomad | rs757091694 |
Varsome | rs757091694 |
LitVar | rs757091694 |
Map | rs757091694 |
PheGenI | rs757091694 |
Biobank | rs757091694 |
1000 genomes | rs757091694 |
hgdp | rs757091694 |
ensembl | rs757091694 |
geneview | rs757091694 |
scholar | rs757091694 |
rs757091694 | |
pharmgkb | rs757091694 |
gwascentral | rs757091694 |
openSNP | rs757091694 |
23andMe | rs757091694 |
SNPshot | rs757091694 |
SNPdbe | rs757091694 |
MSV3d | rs757091694 |
GWAS Ctlg | rs757091694 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs757091694(C;C) |
Alt | rs757091694(C;C) |
Reference | Rs757091694(T;T) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | WDR62 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000019.9:g.36558808T>C |
CLNSRC | |
CLNACC | RCV000413566.1, |