rs142146981
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;T) | 3 | Carrier of an autosomal recessive polycystic kidney disease mutation |
(T;T) | 0 | common/normal |
Make rs142146981(C;C) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 6 |
Position | 51748375 |
Gene | PKHD1 |
is a | snp |
is | mentioned by |
dbSNP | rs142146981 |
dbSNP (classic) | rs142146981 |
ClinGen | rs142146981 |
ebi | rs142146981 |
HLI | rs142146981 |
Exac | rs142146981 |
Gnomad | rs142146981 |
Varsome | rs142146981 |
LitVar | rs142146981 |
Map | rs142146981 |
PheGenI | rs142146981 |
Biobank | rs142146981 |
1000 genomes | rs142146981 |
hgdp | rs142146981 |
ensembl | rs142146981 |
geneview | rs142146981 |
scholar | rs142146981 |
rs142146981 | |
pharmgkb | rs142146981 |
gwascentral | rs142146981 |
openSNP | rs142146981 |
23andMe | rs142146981 |
SNPshot | rs142146981 |
SNPdbe | rs142146981 |
MSV3d | rs142146981 |
GWAS Ctlg | rs142146981 |
Max Magnitude | 3 |