rs868562051
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;G) | 3 | Carrier of an autosomal recessive polycystic kidney disease mutation |
(G;G) | 0 | common/normal |
Make rs868562051(-;-) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 6 |
Position | 52079907 |
Gene | PKHD1 |
is a | snp |
is | mentioned by |
dbSNP | rs868562051 |
dbSNP (classic) | rs868562051 |
ClinGen | rs868562051 |
ebi | rs868562051 |
HLI | rs868562051 |
Exac | rs868562051 |
Gnomad | rs868562051 |
Varsome | rs868562051 |
LitVar | rs868562051 |
Map | rs868562051 |
PheGenI | rs868562051 |
Biobank | rs868562051 |
1000 genomes | rs868562051 |
hgdp | rs868562051 |
ensembl | rs868562051 |
geneview | rs868562051 |
scholar | rs868562051 |
rs868562051 | |
pharmgkb | rs868562051 |
gwascentral | rs868562051 |
openSNP | rs868562051 |
23andMe | rs868562051 |
SNPshot | rs868562051 |
SNPdbe | rs868562051 |
MSV3d | rs868562051 |
GWAS Ctlg | rs868562051 |
Max Magnitude | 3 |