rs199476099
From SNPedia
Polycystic Kidney disease |
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
(G;T) | 5 | Polycystic Kidney Disease (predicted) |
Make rs199476099(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 2118021 |
Gene | PKD1 |
is a | snp |
is | mentioned by |
dbSNP | rs199476099 |
dbSNP (classic) | rs199476099 |
ClinGen | rs199476099 |
ebi | rs199476099 |
HLI | rs199476099 |
Exac | rs199476099 |
Gnomad | rs199476099 |
Varsome | rs199476099 |
LitVar | rs199476099 |
Map | rs199476099 |
PheGenI | rs199476099 |
Biobank | rs199476099 |
1000 genomes | rs199476099 |
hgdp | rs199476099 |
ensembl | rs199476099 |
geneview | rs199476099 |
scholar | rs199476099 |
rs199476099 | |
pharmgkb | rs199476099 |
gwascentral | rs199476099 |
openSNP | rs199476099 |
23andMe | rs199476099 |
SNPshot | rs199476099 |
SNPdbe | rs199476099 |
MSV3d | rs199476099 |
GWAS Ctlg | rs199476099 |
Max Magnitude | 5 |
Polycystic Kidney disease; see OMIM 601313.0011
c.971G>T (p.Arg324Leu)
ClinVar | |
---|---|
Risk | rs199476099(A;A) rs199476099(T;T) |
Alt | rs199476099(A;A) rs199476099(T;T) |
Reference | Rs199476099(G;G) |
Significance | Pathogenic |
Disease | Polycystic kidney disease |
Variation | info |
Gene | PKD1 |
CLNDBN | Polycystic kidney disease, adult type |
Reversed | 1 |
HGVS | NC_000016.9:g.2168022C>A |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000008688.3, |