rs758527425
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs758527425(C;T) |
Make rs758527425(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 18 |
Position | 31089461 |
Gene | DSC2 |
is a | snp |
is | mentioned by |
dbSNP | rs758527425 |
dbSNP (classic) | rs758527425 |
ClinGen | rs758527425 |
ebi | rs758527425 |
HLI | rs758527425 |
Exac | rs758527425 |
Gnomad | rs758527425 |
Varsome | rs758527425 |
LitVar | rs758527425 |
Map | rs758527425 |
PheGenI | rs758527425 |
Biobank | rs758527425 |
1000 genomes | rs758527425 |
hgdp | rs758527425 |
ensembl | rs758527425 |
geneview | rs758527425 |
scholar | rs758527425 |
rs758527425 | |
pharmgkb | rs758527425 |
gwascentral | rs758527425 |
openSNP | rs758527425 |
23andMe | rs758527425 |
SNPshot | rs758527425 |
SNPdbe | rs758527425 |
MSV3d | rs758527425 |
GWAS Ctlg | rs758527425 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs758527425(T;T) |
Alt | rs758527425(T;T) |
Reference | Rs758527425(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | DSC2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000018.9:g.28669424C>T |
CLNSRC | |
CLNACC | RCV000413449.1, |