rs180177249
From SNPedia
Merged into | rs180177248 |
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs180177249(C;T) |
Make rs180177249(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 240873996 |
Gene | AGXT |
is a | snp |
is | mentioned by |
dbSNP | rs180177249 |
dbSNP (classic) | rs180177249 |
ClinGen | rs180177249 |
ebi | rs180177249 |
HLI | rs180177249 |
Exac | rs180177249 |
Gnomad | rs180177249 |
Varsome | rs180177249 |
LitVar | rs180177249 |
Map | rs180177249 |
PheGenI | rs180177249 |
Biobank | rs180177249 |
1000 genomes | rs180177249 |
hgdp | rs180177249 |
ensembl | rs180177249 |
geneview | rs180177249 |
scholar | rs180177249 |
rs180177249 | |
pharmgkb | rs180177249 |
gwascentral | rs180177249 |
openSNP | rs180177249 |
23andMe | rs180177249 |
SNPshot | rs180177249 |
SNPdbe | rs180177249 |
MSV3d | rs180177249 |
GWAS Ctlg | rs180177249 |
Status | Merged into rs180177248 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs180177249(T;T) |
Alt | rs180177249(T;T) |
Reference | Rs180177249(C;C) |
Significance | Pathogenic |
Disease | |
Variation | info |
Gene | AGXT |
CLNDBN | OMIM |
Reversed | 0 |
HGVS | NC_000002.11:g.241813413C>T |
CLNSRC | |
CLNACC |