rs115735611
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs115735611(A;G) |
Make rs115735611(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 232791426 |
Gene | GIGYF2 |
is a | snp |
is | mentioned by |
dbSNP | rs115735611 |
dbSNP (classic) | rs115735611 |
ClinGen | rs115735611 |
ebi | rs115735611 |
HLI | rs115735611 |
Exac | rs115735611 |
Gnomad | rs115735611 |
Varsome | rs115735611 |
LitVar | rs115735611 |
Map | rs115735611 |
PheGenI | rs115735611 |
Biobank | rs115735611 |
1000 genomes | rs115735611 |
hgdp | rs115735611 |
ensembl | rs115735611 |
geneview | rs115735611 |
scholar | rs115735611 |
rs115735611 | |
pharmgkb | rs115735611 |
gwascentral | rs115735611 |
openSNP | rs115735611 |
23andMe | rs115735611 |
SNPshot | rs115735611 |
SNPdbe | rs115735611 |
MSV3d | rs115735611 |
GWAS Ctlg | rs115735611 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs115735611(G;G) |
Alt | rs115735611(G;G) |
Reference | Rs115735611(A;A) |
Significance | Other |
Disease | Parkinson disease 11 |
Variation | info |
Gene | GIGYF2 |
CLNDBN | Parkinson disease 11 |
Reversed | 0 |
HGVS | NC_000002.11:g.233656136A>G |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000000793.5, |