rs752432726
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs752432726(A;G) |
Make rs752432726(G;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 18 |
Position | 31524754 |
Gene | DSG2 |
is a | snp |
is | mentioned by |
dbSNP | rs752432726 |
dbSNP (classic) | rs752432726 |
ClinGen | rs752432726 |
ebi | rs752432726 |
HLI | rs752432726 |
Exac | rs752432726 |
Gnomad | rs752432726 |
Varsome | rs752432726 |
LitVar | rs752432726 |
Map | rs752432726 |
PheGenI | rs752432726 |
Biobank | rs752432726 |
1000 genomes | rs752432726 |
hgdp | rs752432726 |
ensembl | rs752432726 |
geneview | rs752432726 |
scholar | rs752432726 |
rs752432726 | |
pharmgkb | rs752432726 |
gwascentral | rs752432726 |
openSNP | rs752432726 |
23andMe | rs752432726 |
SNPshot | rs752432726 |
SNPdbe | rs752432726 |
MSV3d | rs752432726 |
GWAS Ctlg | rs752432726 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs752432726(G;G) |
Alt | rs752432726(G;G) |
Reference | Rs752432726(A;A) |
Significance | Pathogenic |
Disease | not specified |
Variation | info |
Gene | DSG2 |
CLNDBN | not specified |
Reversed | 0 |
HGVS | NC_000018.9:g.29104717A>G |
CLNSRC | |
CLNACC | RCV000455978.1, |