rs139969658
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs139969658(C;T) |
Make rs139969658(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 6 |
Position | 7585738 |
Gene | DSP |
is a | snp |
is | mentioned by |
dbSNP | rs139969658 |
dbSNP (classic) | rs139969658 |
ClinGen | rs139969658 |
ebi | rs139969658 |
HLI | rs139969658 |
Exac | rs139969658 |
Gnomad | rs139969658 |
Varsome | rs139969658 |
LitVar | rs139969658 |
Map | rs139969658 |
PheGenI | rs139969658 |
Biobank | rs139969658 |
1000 genomes | rs139969658 |
hgdp | rs139969658 |
ensembl | rs139969658 |
geneview | rs139969658 |
scholar | rs139969658 |
rs139969658 | |
pharmgkb | rs139969658 |
gwascentral | rs139969658 |
openSNP | rs139969658 |
23andMe | rs139969658 |
SNPshot | rs139969658 |
SNPdbe | rs139969658 |
MSV3d | rs139969658 |
GWAS Ctlg | rs139969658 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs139969658(T;T) |
Alt | rs139969658(T;T) |
Reference | Rs139969658(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | DSP |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000006.11:g.7585971C>T |
CLNSRC | |
CLNACC | RCV000181351.2, |