rs768858918
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs768858918(A;A) |
Make rs768858918(A;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 6 |
Position | 7577886 |
Gene | DSP |
is a | snp |
is | mentioned by |
dbSNP | rs768858918 |
dbSNP (classic) | rs768858918 |
ClinGen | rs768858918 |
ebi | rs768858918 |
HLI | rs768858918 |
Exac | rs768858918 |
Gnomad | rs768858918 |
Varsome | rs768858918 |
LitVar | rs768858918 |
Map | rs768858918 |
PheGenI | rs768858918 |
Biobank | rs768858918 |
1000 genomes | rs768858918 |
hgdp | rs768858918 |
ensembl | rs768858918 |
geneview | rs768858918 |
scholar | rs768858918 |
rs768858918 | |
pharmgkb | rs768858918 |
gwascentral | rs768858918 |
openSNP | rs768858918 |
23andMe | rs768858918 |
SNPshot | rs768858918 |
SNPdbe | rs768858918 |
MSV3d | rs768858918 |
GWAS Ctlg | rs768858918 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs768858918(A;A) |
Alt | rs768858918(A;A) |
Reference | Rs768858918(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | DSP |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000006.11:g.7578119G>A |
CLNSRC | |
CLNACC | RCV000181311.2, |