rs606231210
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs606231210(-;-) |
Make rs606231210(-;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 6 |
Position | 160741418 |
Gene | PLG |
is a | snp |
is | mentioned by |
dbSNP | rs606231210 |
dbSNP (classic) | rs606231210 |
ClinGen | rs606231210 |
ebi | rs606231210 |
HLI | rs606231210 |
Exac | rs606231210 |
Gnomad | rs606231210 |
Varsome | rs606231210 |
LitVar | rs606231210 |
Map | rs606231210 |
PheGenI | rs606231210 |
Biobank | rs606231210 |
1000 genomes | rs606231210 |
hgdp | rs606231210 |
ensembl | rs606231210 |
geneview | rs606231210 |
scholar | rs606231210 |
rs606231210 | |
pharmgkb | rs606231210 |
gwascentral | rs606231210 |
openSNP | rs606231210 |
23andMe | rs606231210 |
SNPshot | rs606231210 |
SNPdbe | rs606231210 |
MSV3d | rs606231210 |
GWAS Ctlg | rs606231210 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs606231210(-;-) |
Alt | rs606231210(-;-) |
Reference | Rs606231210(G;G) |
Significance | Pathogenic |
Disease | Plasminogen deficiency |
Variation | info |
Gene | PLG |
CLNDBN | Plasminogen deficiency, type I |
Reversed | 0 |
HGVS | NC_000006.11:g.161162450delG |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000014550.26, |