rs786205596
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs786205596(A;C) |
Make rs786205596(C;C) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 9 |
Position | 368196 |
Gene | DOCK8 |
is a | snp |
is | mentioned by |
dbSNP | rs786205596 |
dbSNP (classic) | rs786205596 |
ClinGen | rs786205596 |
ebi | rs786205596 |
HLI | rs786205596 |
Exac | rs786205596 |
Gnomad | rs786205596 |
Varsome | rs786205596 |
LitVar | rs786205596 |
Map | rs786205596 |
PheGenI | rs786205596 |
Biobank | rs786205596 |
1000 genomes | rs786205596 |
hgdp | rs786205596 |
ensembl | rs786205596 |
geneview | rs786205596 |
scholar | rs786205596 |
rs786205596 | |
pharmgkb | rs786205596 |
gwascentral | rs786205596 |
openSNP | rs786205596 |
23andMe | rs786205596 |
SNPshot | rs786205596 |
SNPdbe | rs786205596 |
MSV3d | rs786205596 |
GWAS Ctlg | rs786205596 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs786205596(C;C) |
Alt | rs786205596(C;C) |
Reference | Rs786205596(A;A) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | DOCK8 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000009.11:g.368196A>C |
CLNSRC | |
CLNACC | RCV000171422.1, |