rs74503222
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;G) | 3 | Carrier of a phenylketonuria mutation |
(G;G) | 0 | common in clinvar |
Make rs74503222(A;A) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 12 |
Position | 102852912 |
Gene | PAH |
is a | snp |
is | mentioned by |
dbSNP | rs74503222 |
dbSNP (classic) | rs74503222 |
ClinGen | rs74503222 |
ebi | rs74503222 |
HLI | rs74503222 |
Exac | rs74503222 |
Gnomad | rs74503222 |
Varsome | rs74503222 |
LitVar | rs74503222 |
Map | rs74503222 |
PheGenI | rs74503222 |
Biobank | rs74503222 |
1000 genomes | rs74503222 |
hgdp | rs74503222 |
ensembl | rs74503222 |
geneview | rs74503222 |
scholar | rs74503222 |
rs74503222 | |
pharmgkb | rs74503222 |
gwascentral | rs74503222 |
openSNP | rs74503222 |
23andMe | rs74503222 |
SNPshot | rs74503222 |
SNPdbe | rs74503222 |
MSV3d | rs74503222 |
GWAS Ctlg | rs74503222 |
Max Magnitude | 3 |
aka c.745C>T (p.Leu249Phe)
FTDNA & MyHeritage name: VG12S8420
ClinVar | |
---|---|
Risk | rs74503222(A;A) |
Alt | rs74503222(A;A) |
Reference | Rs74503222(G;G) |
Significance | Pathogenic |
Disease | not provided Phenylketonuria |
Variation | info |
Gene | PAH |
CLNDBN | not provided Phenylketonuria |
Reversed | 0 |
HGVS | NC_000012.11:g.103246690G>A |
CLNSRC | HGMD UniProtKB (protein) |
CLNACC | RCV000089076.3, RCV000153634.3, |