rs794728157
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs794728157(-;TT) |
Make rs794728157(TT;TT) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 6 |
Position | 7578528 |
Gene | DSP |
is a | snp |
is | mentioned by |
dbSNP | rs794728157 |
dbSNP (classic) | rs794728157 |
ClinGen | rs794728157 |
ebi | rs794728157 |
HLI | rs794728157 |
Exac | rs794728157 |
Gnomad | rs794728157 |
Varsome | rs794728157 |
LitVar | rs794728157 |
Map | rs794728157 |
PheGenI | rs794728157 |
Biobank | rs794728157 |
1000 genomes | rs794728157 |
hgdp | rs794728157 |
ensembl | rs794728157 |
geneview | rs794728157 |
scholar | rs794728157 |
rs794728157 | |
pharmgkb | rs794728157 |
gwascentral | rs794728157 |
openSNP | rs794728157 |
23andMe | rs794728157 |
SNPshot | rs794728157 |
SNPdbe | rs794728157 |
MSV3d | rs794728157 |
GWAS Ctlg | rs794728157 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs794728157(TT;TT) |
Alt | rs794728157(TT;TT) |
Reference | Rs794728157(-;-) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | DSP |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000006.11:g.7578760_7578761dupTT |
CLNSRC | |
CLNACC | RCV000181392.1, |