rs786205659
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs786205659(-;-) |
Make rs786205659(-;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 9 |
Position | 69225352 |
Gene | TJP2 |
is a | snp |
is | mentioned by |
dbSNP | rs786205659 |
dbSNP (classic) | rs786205659 |
ClinGen | rs786205659 |
ebi | rs786205659 |
HLI | rs786205659 |
Exac | rs786205659 |
Gnomad | rs786205659 |
Varsome | rs786205659 |
LitVar | rs786205659 |
Map | rs786205659 |
PheGenI | rs786205659 |
Biobank | rs786205659 |
1000 genomes | rs786205659 |
hgdp | rs786205659 |
ensembl | rs786205659 |
geneview | rs786205659 |
scholar | rs786205659 |
rs786205659 | |
pharmgkb | rs786205659 |
gwascentral | rs786205659 |
openSNP | rs786205659 |
23andMe | rs786205659 |
SNPshot | rs786205659 |
SNPdbe | rs786205659 |
MSV3d | rs786205659 |
GWAS Ctlg | rs786205659 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs786205659(-;-) |
Alt | rs786205659(-;-) |
Reference | Rs786205659(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | TJP2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000009.11:g.71840268delG |
CLNSRC | |
CLNACC | RCV000171538.1, |