rs143321486
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs143321486(C;G) |
Make rs143321486(G;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 17 |
Position | 42911295 |
Gene | G6PC |
is a | snp |
is | mentioned by |
dbSNP | rs143321486 |
dbSNP (classic) | rs143321486 |
ClinGen | rs143321486 |
ebi | rs143321486 |
HLI | rs143321486 |
Exac | rs143321486 |
Gnomad | rs143321486 |
Varsome | rs143321486 |
LitVar | rs143321486 |
Map | rs143321486 |
PheGenI | rs143321486 |
Biobank | rs143321486 |
1000 genomes | rs143321486 |
hgdp | rs143321486 |
ensembl | rs143321486 |
geneview | rs143321486 |
scholar | rs143321486 |
rs143321486 | |
pharmgkb | rs143321486 |
gwascentral | rs143321486 |
openSNP | rs143321486 |
23andMe | rs143321486 |
SNPshot | rs143321486 |
SNPdbe | rs143321486 |
MSV3d | rs143321486 |
GWAS Ctlg | rs143321486 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs143321486(G;G) |
Alt | rs143321486(G;G) |
Reference | Rs143321486(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | G6PC |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000017.10:g.41063312C>G |
CLNSRC | |
CLNACC | RCV000199189.1, |