rs116074753
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs116074753(A;C) |
Make rs116074753(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 232794835 |
Gene | GIGYF2 |
is a | snp |
is | mentioned by |
dbSNP | rs116074753 |
dbSNP (classic) | rs116074753 |
ClinGen | rs116074753 |
ebi | rs116074753 |
HLI | rs116074753 |
Exac | rs116074753 |
Gnomad | rs116074753 |
Varsome | rs116074753 |
LitVar | rs116074753 |
Map | rs116074753 |
PheGenI | rs116074753 |
Biobank | rs116074753 |
1000 genomes | rs116074753 |
hgdp | rs116074753 |
ensembl | rs116074753 |
geneview | rs116074753 |
scholar | rs116074753 |
rs116074753 | |
pharmgkb | rs116074753 |
gwascentral | rs116074753 |
openSNP | rs116074753 |
23andMe | rs116074753 |
SNPshot | rs116074753 |
SNPdbe | rs116074753 |
MSV3d | rs116074753 |
GWAS Ctlg | rs116074753 |
GMAF | 0.0004591 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs116074753(C;C) rs116074753(G;G) |
Alt | rs116074753(C;C) rs116074753(G;G) |
Reference | Rs116074753(A;A) |
Significance | Other |
Disease | Parkinson disease 11 |
Variation | info |
Gene | GIGYF2 |
CLNDBN | Parkinson disease 11 |
Reversed | 0 |
HGVS | NC_000002.11:g.233659545A>C |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000000790.5, |