rs62514934
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
(A;G) | 3 | Carrier of a phenylketonuria mutation |
Make rs62514934(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 102855180 |
Gene | PAH |
is a | snp |
is | mentioned by |
dbSNP | rs62514934 |
dbSNP (classic) | rs62514934 |
ClinGen | rs62514934 |
ebi | rs62514934 |
HLI | rs62514934 |
Exac | rs62514934 |
Gnomad | rs62514934 |
Varsome | rs62514934 |
LitVar | rs62514934 |
Map | rs62514934 |
PheGenI | rs62514934 |
Biobank | rs62514934 |
1000 genomes | rs62514934 |
hgdp | rs62514934 |
ensembl | rs62514934 |
geneview | rs62514934 |
scholar | rs62514934 |
rs62514934 | |
pharmgkb | rs62514934 |
gwascentral | rs62514934 |
openSNP | rs62514934 |
23andMe | rs62514934 |
SNPshot | rs62514934 |
SNPdbe | rs62514934 |
MSV3d | rs62514934 |
GWAS Ctlg | rs62514934 |
Max Magnitude | 3 |
ClinVar | |
---|---|
Risk | rs62514934(G;G) |
Alt | rs62514934(G;G) |
Reference | Rs62514934(A;A) |
Significance | Pathogenic |
Disease | Phenylketonuria not provided |
Variation | info |
Gene | PAH |
CLNDBN | Phenylketonuria not provided |
Reversed | 1 |
HGVS | NC_000012.11:g.103248958T>C |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000000640.3, RCV000089024.1, |