rs766251466
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(GAG;GAG) | 0 | common in clinvar |
Make rs766251466(-;-) |
Make rs766251466(-;GAG) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 20 |
Position | 3916956 |
Gene | MIR103A2, PANK2 |
is a | snp |
is | mentioned by |
dbSNP | rs766251466 |
dbSNP (classic) | rs766251466 |
ClinGen | rs766251466 |
ebi | rs766251466 |
HLI | rs766251466 |
Exac | rs766251466 |
Gnomad | rs766251466 |
Varsome | rs766251466 |
LitVar | rs766251466 |
Map | rs766251466 |
PheGenI | rs766251466 |
Biobank | rs766251466 |
1000 genomes | rs766251466 |
hgdp | rs766251466 |
ensembl | rs766251466 |
geneview | rs766251466 |
scholar | rs766251466 |
rs766251466 | |
pharmgkb | rs766251466 |
gwascentral | rs766251466 |
openSNP | rs766251466 |
23andMe | rs766251466 |
SNPshot | rs766251466 |
SNPdbe | rs766251466 |
MSV3d | rs766251466 |
GWAS Ctlg | rs766251466 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs766251466(-;-) |
Alt | rs766251466(-;-) |
Reference | Rs766251466(GAG;GAG) |
Significance | Pathogenic |
Disease | Pigmentary pallidal degeneration |
Variation | info |
Gene | MIR103A2 PANK2 |
CLNDBN | Pigmentary pallidal degeneration |
Reversed | 0 |
HGVS | NC_000020.10:g.3897603_3897605delGAG |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000004822.2, |