rs758282201
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs758282201(-;-) |
Make rs758282201(-;A) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 18 |
Position | 31519812 |
Gene | DSG2 |
is a | snp |
is | mentioned by |
dbSNP | rs758282201 |
dbSNP (classic) | rs758282201 |
ClinGen | rs758282201 |
ebi | rs758282201 |
HLI | rs758282201 |
Exac | rs758282201 |
Gnomad | rs758282201 |
Varsome | rs758282201 |
LitVar | rs758282201 |
Map | rs758282201 |
PheGenI | rs758282201 |
Biobank | rs758282201 |
1000 genomes | rs758282201 |
hgdp | rs758282201 |
ensembl | rs758282201 |
geneview | rs758282201 |
scholar | rs758282201 |
rs758282201 | |
pharmgkb | rs758282201 |
gwascentral | rs758282201 |
openSNP | rs758282201 |
23andMe | rs758282201 |
SNPshot | rs758282201 |
SNPdbe | rs758282201 |
MSV3d | rs758282201 |
GWAS Ctlg | rs758282201 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs758282201(-;-) |
Alt | rs758282201(-;-) |
Reference | Rs758282201(A;A) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | DSG2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000018.9:g.29099775delA |
CLNSRC | |
CLNACC | RCV000480668.1, |