rs1020621286
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 6 |
Position | 51772791 |
Gene | PKHD1 |
is a | snp |
is | mentioned by |
dbSNP | rs1020621286 |
dbSNP (classic) | rs1020621286 |
ClinGen | rs1020621286 |
ebi | rs1020621286 |
HLI | rs1020621286 |
Exac | rs1020621286 |
Gnomad | rs1020621286 |
Varsome | rs1020621286 |
LitVar | rs1020621286 |
Map | rs1020621286 |
PheGenI | rs1020621286 |
Biobank | rs1020621286 |
1000 genomes | rs1020621286 |
hgdp | rs1020621286 |
ensembl | rs1020621286 |
geneview | rs1020621286 |
scholar | rs1020621286 |
rs1020621286 | |
pharmgkb | rs1020621286 |
gwascentral | rs1020621286 |
openSNP | rs1020621286 |
23andMe | rs1020621286 |
SNPshot | rs1020621286 |
SNPdbe | rs1020621286 |
MSV3d | rs1020621286 |
GWAS Ctlg | rs1020621286 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1020621286(G;G) |
Alt | rs1020621286(G;G) |
Reference | Rs1020621286(T;T) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | PKHD1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000006.11:g.51637589T>G |
CLNSRC | |
CLNACC | RCV000492982.1, |