rs62507283
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;G) | 3 | Carrier of a phenylketonuria mutation |
(G;G) | 0 | common in clinvar |
(G;T) | 3 | Carrier of a phenylketonuria mutation |
Make rs62507283(C;C) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 12 |
Position | 102852941 |
Gene | PAH |
is a | snp |
is | mentioned by |
dbSNP | rs62507283 |
dbSNP (classic) | rs62507283 |
ClinGen | rs62507283 |
ebi | rs62507283 |
HLI | rs62507283 |
Exac | rs62507283 |
Gnomad | rs62507283 |
Varsome | rs62507283 |
LitVar | rs62507283 |
Map | rs62507283 |
PheGenI | rs62507283 |
Biobank | rs62507283 |
1000 genomes | rs62507283 |
hgdp | rs62507283 |
ensembl | rs62507283 |
geneview | rs62507283 |
scholar | rs62507283 |
rs62507283 | |
pharmgkb | rs62507283 |
gwascentral | rs62507283 |
openSNP | rs62507283 |
23andMe | rs62507283 |
SNPshot | rs62507283 |
SNPdbe | rs62507283 |
MSV3d | rs62507283 |
GWAS Ctlg | rs62507283 |
Max Magnitude | 3 |
ClinVar | |
---|---|
Risk | rs62507283(A;A) rs62507283(C;C) rs62507283(T;T) |
Alt | rs62507283(A;A) rs62507283(C;C) rs62507283(T;T) |
Reference | Rs62507283(G;G) |
Significance | Untested |
Disease | not provided not specified |
Variation | info |
Gene | PAH |
CLNDBN | not provided not specified |
Reversed | 1 |
HGVS | NC_000012.11:g.103246719C>A; NC_000012.11:g.103246719C>G; NC_000012.11:g.103246719C>T |
CLNSRC | HGMD |
CLNACC | RCV000089051.5, RCV000259121.1, RCV000089050.1, RCV000089049.1, |