rs762879569
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs762879569(A;A) |
Make rs762879569(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 20 |
Position | 3907941 |
Gene | PANK2 |
is a | snp |
is | mentioned by |
dbSNP | rs762879569 |
dbSNP (classic) | rs762879569 |
ClinGen | rs762879569 |
ebi | rs762879569 |
HLI | rs762879569 |
Exac | rs762879569 |
Gnomad | rs762879569 |
Varsome | rs762879569 |
LitVar | rs762879569 |
Map | rs762879569 |
PheGenI | rs762879569 |
Biobank | rs762879569 |
1000 genomes | rs762879569 |
hgdp | rs762879569 |
ensembl | rs762879569 |
geneview | rs762879569 |
scholar | rs762879569 |
rs762879569 | |
pharmgkb | rs762879569 |
gwascentral | rs762879569 |
openSNP | rs762879569 |
23andMe | rs762879569 |
SNPshot | rs762879569 |
SNPdbe | rs762879569 |
MSV3d | rs762879569 |
GWAS Ctlg | rs762879569 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs762879569(A;A) |
Alt | rs762879569(A;A) |
Reference | Rs762879569(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | PANK2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000020.10:g.3888588G>A |
CLNSRC | |
CLNACC | RCV000493982.1, |