rs1060499709
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs1060499709(A;A) |
Make rs1060499709(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 17 |
Position | 56856582 |
Gene | DGKE |
is a | snp |
is | mentioned by |
dbSNP | rs1060499709 |
dbSNP (classic) | rs1060499709 |
ClinGen | rs1060499709 |
ebi | rs1060499709 |
HLI | rs1060499709 |
Exac | rs1060499709 |
Gnomad | rs1060499709 |
Varsome | rs1060499709 |
LitVar | rs1060499709 |
Map | rs1060499709 |
PheGenI | rs1060499709 |
Biobank | rs1060499709 |
1000 genomes | rs1060499709 |
hgdp | rs1060499709 |
ensembl | rs1060499709 |
geneview | rs1060499709 |
scholar | rs1060499709 |
rs1060499709 | |
pharmgkb | rs1060499709 |
gwascentral | rs1060499709 |
openSNP | rs1060499709 |
23andMe | rs1060499709 |
SNPshot | rs1060499709 |
SNPdbe | rs1060499709 |
MSV3d | rs1060499709 |
GWAS Ctlg | rs1060499709 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1060499709(A;A) |
Alt | rs1060499709(A;A) |
Reference | Rs1060499709(G;G) |
Significance | Probable-Pathogenic |
Disease | Nephrotic syndrome |
Variation | info |
Gene | DGKE |
CLNDBN | Nephrotic syndrome, type 7 |
Reversed | 0 |
HGVS | NC_000017.10:g.54933943G>A |
CLNSRC | |
CLNACC | RCV000449615.1, |