rs5030654
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(-;G) | 3 | Carrier of a phenylketonuria mutation |
(G;G) | 0 | common in clinvar |
Make rs5030654(-;-) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 12 |
Position | 102843756 |
Gene | PAH |
is a | snp |
is | mentioned by |
dbSNP | rs5030654 |
dbSNP (classic) | rs5030654 |
ClinGen | rs5030654 |
ebi | rs5030654 |
HLI | rs5030654 |
Exac | rs5030654 |
Gnomad | rs5030654 |
Varsome | rs5030654 |
LitVar | rs5030654 |
Map | rs5030654 |
PheGenI | rs5030654 |
Biobank | rs5030654 |
1000 genomes | rs5030654 |
hgdp | rs5030654 |
ensembl | rs5030654 |
geneview | rs5030654 |
scholar | rs5030654 |
rs5030654 | |
pharmgkb | rs5030654 |
gwascentral | rs5030654 |
openSNP | rs5030654 |
23andMe | rs5030654 |
SNPshot | rs5030654 |
SNPdbe | rs5030654 |
MSV3d | rs5030654 |
GWAS Ctlg | rs5030654 |
Max Magnitude | 3 |
ClinVar | |
---|---|
Risk | rs5030654(-;-) |
Alt | rs5030654(-;-) |
Reference | Rs5030654(G;G) |
Significance | Pathogenic |
Disease | not provided Phenylketonuria |
Variation | info |
Gene | PAH |
CLNDBN | not provided Phenylketonuria |
Reversed | 1 |
HGVS | NC_000012.11:g.103237534delC |
CLNSRC | |
CLNACC | RCV000088751.1, RCV000169397.1, |