rs1064794616
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(TAT;TAT) | 0 | common in clinvar |
Chromosome | 6 |
Position | 7579605 |
Gene | DSP |
is a | snp |
is | mentioned by |
dbSNP | rs1064794616 |
dbSNP (classic) | rs1064794616 |
ClinGen | rs1064794616 |
ebi | rs1064794616 |
HLI | rs1064794616 |
Exac | rs1064794616 |
Gnomad | rs1064794616 |
Varsome | rs1064794616 |
LitVar | rs1064794616 |
Map | rs1064794616 |
PheGenI | rs1064794616 |
Biobank | rs1064794616 |
1000 genomes | rs1064794616 |
hgdp | rs1064794616 |
ensembl | rs1064794616 |
geneview | rs1064794616 |
scholar | rs1064794616 |
rs1064794616 | |
pharmgkb | rs1064794616 |
gwascentral | rs1064794616 |
openSNP | rs1064794616 |
23andMe | rs1064794616 |
SNPshot | rs1064794616 |
SNPdbe | rs1064794616 |
MSV3d | rs1064794616 |
GWAS Ctlg | rs1064794616 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1064794616(G;G) |
Alt | rs1064794616(G;G) |
Reference | Rs1064794616(TAT;TAT) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | DSP |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000006.11:g.7579838_7579840delTATinsG |
CLNSRC | |
CLNACC | RCV000478280.1, |