rs774863785
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs774863785(A;A) |
Make rs774863785(A;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 18 |
Position | 31531167 |
Gene | DSG2 |
is a | snp |
is | mentioned by |
dbSNP | rs774863785 |
dbSNP (classic) | rs774863785 |
ClinGen | rs774863785 |
ebi | rs774863785 |
HLI | rs774863785 |
Exac | rs774863785 |
Gnomad | rs774863785 |
Varsome | rs774863785 |
LitVar | rs774863785 |
Map | rs774863785 |
PheGenI | rs774863785 |
Biobank | rs774863785 |
1000 genomes | rs774863785 |
hgdp | rs774863785 |
ensembl | rs774863785 |
geneview | rs774863785 |
scholar | rs774863785 |
rs774863785 | |
pharmgkb | rs774863785 |
gwascentral | rs774863785 |
openSNP | rs774863785 |
23andMe | rs774863785 |
SNPshot | rs774863785 |
SNPdbe | rs774863785 |
MSV3d | rs774863785 |
GWAS Ctlg | rs774863785 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs774863785(A;A) |
Alt | rs774863785(A;A) |
Reference | Rs774863785(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | DSG2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000018.9:g.29111130G>A |
CLNSRC | |
CLNACC | RCV000181216.2, |