rs62508695
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs62508695(A;A) |
Make rs62508695(A;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 12 |
Position | 102894875 |
Gene | PAH |
is a | snp |
is | mentioned by |
dbSNP | rs62508695 |
dbSNP (classic) | rs62508695 |
ClinGen | rs62508695 |
ebi | rs62508695 |
HLI | rs62508695 |
Exac | rs62508695 |
Gnomad | rs62508695 |
Varsome | rs62508695 |
LitVar | rs62508695 |
Map | rs62508695 |
PheGenI | rs62508695 |
Biobank | rs62508695 |
1000 genomes | rs62508695 |
hgdp | rs62508695 |
ensembl | rs62508695 |
geneview | rs62508695 |
scholar | rs62508695 |
rs62508695 | |
pharmgkb | rs62508695 |
gwascentral | rs62508695 |
openSNP | rs62508695 |
23andMe | rs62508695 |
SNPshot | rs62508695 |
SNPdbe | rs62508695 |
MSV3d | rs62508695 |
GWAS Ctlg | rs62508695 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs62508695(A;A) |
Alt | rs62508695(A;A) |
Reference | Rs62508695(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.103288653C>T |
CLNSRC | |
CLNACC | RCV000088876.3, RCV000212762.1, |