rs121918126
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs121918126(C;C) |
Make rs121918126(C;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 55698005 |
Gene | SLC6A2 |
is a | snp |
is | mentioned by |
dbSNP | rs121918126 |
dbSNP (classic) | rs121918126 |
ClinGen | rs121918126 |
ebi | rs121918126 |
HLI | rs121918126 |
Exac | rs121918126 |
Gnomad | rs121918126 |
Varsome | rs121918126 |
LitVar | rs121918126 |
Map | rs121918126 |
PheGenI | rs121918126 |
Biobank | rs121918126 |
1000 genomes | rs121918126 |
hgdp | rs121918126 |
ensembl | rs121918126 |
geneview | rs121918126 |
scholar | rs121918126 |
rs121918126 | |
pharmgkb | rs121918126 |
gwascentral | rs121918126 |
openSNP | rs121918126 |
23andMe | rs121918126 |
SNPshot | rs121918126 |
SNPdbe | rs121918126 |
MSV3d | rs121918126 |
GWAS Ctlg | rs121918126 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs121918126(A;A) rs121918126(C;C) rs121918126(T;T) |
Alt | rs121918126(A;A) rs121918126(C;C) rs121918126(T;T) |
Reference | Rs121918126(G;G) |
Significance | Pathogenic |
Disease | Orthostatic intolerance |
Variation | info |
Gene | SLC6A2 |
CLNDBN | Orthostatic intolerance |
Reversed | 0 |
HGVS | NC_000016.9:g.55731917G>C |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000015043.25, |