rs121917810
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs121917810(G;T) |
Make rs121917810(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | X |
Position | 116172342 |
Gene | AGTR2 |
is a | snp |
is | mentioned by |
dbSNP | rs121917810 |
dbSNP (classic) | rs121917810 |
ClinGen | rs121917810 |
ebi | rs121917810 |
HLI | rs121917810 |
Exac | rs121917810 |
Gnomad | rs121917810 |
Varsome | rs121917810 |
LitVar | rs121917810 |
Map | rs121917810 |
PheGenI | rs121917810 |
Biobank | rs121917810 |
1000 genomes | rs121917810 |
hgdp | rs121917810 |
ensembl | rs121917810 |
geneview | rs121917810 |
scholar | rs121917810 |
rs121917810 | |
pharmgkb | rs121917810 |
gwascentral | rs121917810 |
openSNP | rs121917810 |
23andMe | rs121917810 |
SNPshot | rs121917810 |
SNPdbe | rs121917810 |
MSV3d | rs121917810 |
GWAS Ctlg | rs121917810 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs121917810(T;T) |
Alt | rs121917810(T;T) |
Reference | Rs121917810(G;G) |
Significance | Non-pathogenic |
Disease | not provided not specified |
Variation | info |
Gene | AGTR2 |
CLNDBN | not provided not specified |
Reversed | 0 |
HGVS | NC_000023.10:g.115303595G>T |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000088651.2, RCV000116283.1, |