rs62644503
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;G) | 3 | Carrier of a phenylketonuria mutation |
(G;G) | 0 | common in clinvar |
Make rs62644503(A;A) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 12 |
Position | 102852902 |
Gene | PAH |
is a | snp |
is | mentioned by |
dbSNP | rs62644503 |
dbSNP (classic) | rs62644503 |
ClinGen | rs62644503 |
ebi | rs62644503 |
HLI | rs62644503 |
Exac | rs62644503 |
Gnomad | rs62644503 |
Varsome | rs62644503 |
LitVar | rs62644503 |
Map | rs62644503 |
PheGenI | rs62644503 |
Biobank | rs62644503 |
1000 genomes | rs62644503 |
hgdp | rs62644503 |
ensembl | rs62644503 |
geneview | rs62644503 |
scholar | rs62644503 |
rs62644503 | |
pharmgkb | rs62644503 |
gwascentral | rs62644503 |
openSNP | rs62644503 |
23andMe | rs62644503 |
SNPshot | rs62644503 |
SNPdbe | rs62644503 |
MSV3d | rs62644503 |
GWAS Ctlg | rs62644503 |
Max Magnitude | 3 |
aka c.755G>A (p.Arg252Gln)
FTDNA & MyHeritage name: VG12S8424
ClinVar | |
---|---|
Risk | rs62644503(A;A) |
Alt | rs62644503(A;A) |
Reference | Rs62644503(G;G) |
Significance | Pathogenic |
Disease | not provided Phenylketonuria |
Variation | info |
Gene | PAH |
CLNDBN | not provided Phenylketonuria |
Reversed | 1 |
HGVS | NC_000012.11:g.103246680C>T |
CLNSRC | UniProtKB (protein) |
CLNACC | RCV000089080.1, RCV000179742.1, |