rs192864327
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs192864327(G;T) |
Make rs192864327(T;T) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 9 |
Position | 271626 |
Gene | DOCK8 |
is a | snp |
is | mentioned by |
dbSNP | rs192864327 |
dbSNP (classic) | rs192864327 |
ClinGen | rs192864327 |
ebi | rs192864327 |
HLI | rs192864327 |
Exac | rs192864327 |
Gnomad | rs192864327 |
Varsome | rs192864327 |
LitVar | rs192864327 |
Map | rs192864327 |
PheGenI | rs192864327 |
Biobank | rs192864327 |
1000 genomes | rs192864327 |
hgdp | rs192864327 |
ensembl | rs192864327 |
geneview | rs192864327 |
scholar | rs192864327 |
rs192864327 | |
pharmgkb | rs192864327 |
gwascentral | rs192864327 |
openSNP | rs192864327 |
23andMe | rs192864327 |
SNPshot | rs192864327 |
SNPdbe | rs192864327 |
MSV3d | rs192864327 |
GWAS Ctlg | rs192864327 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs192864327(T;T) |
Alt | rs192864327(T;T) |
Reference | Rs192864327(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | DOCK8 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000009.11:g.271626G>T |
CLNSRC | |
CLNACC | RCV000256030.2, |