rs776731688
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs776731688(A;A) |
Make rs776731688(A;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 17 |
Position | 35577384 |
Gene | PEX12 |
is a | snp |
is | mentioned by |
dbSNP | rs776731688 |
dbSNP (classic) | rs776731688 |
ClinGen | rs776731688 |
ebi | rs776731688 |
HLI | rs776731688 |
Exac | rs776731688 |
Gnomad | rs776731688 |
Varsome | rs776731688 |
LitVar | rs776731688 |
Map | rs776731688 |
PheGenI | rs776731688 |
Biobank | rs776731688 |
1000 genomes | rs776731688 |
hgdp | rs776731688 |
ensembl | rs776731688 |
geneview | rs776731688 |
scholar | rs776731688 |
rs776731688 | |
pharmgkb | rs776731688 |
gwascentral | rs776731688 |
openSNP | rs776731688 |
23andMe | rs776731688 |
SNPshot | rs776731688 |
SNPdbe | rs776731688 |
MSV3d | rs776731688 |
GWAS Ctlg | rs776731688 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs776731688(A;A) |
Alt | rs776731688(A;A) |
Reference | Rs776731688(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | PEX12 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000017.10:g.33904403G>A |
CLNSRC | |
CLNACC | RCV000171254.1, |