rs188698686
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs188698686(A;G) |
Make rs188698686(G;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 5 |
Position | 132385369 |
Gene | SLC22A5 |
is a | snp |
is | mentioned by |
dbSNP | rs188698686 |
dbSNP (classic) | rs188698686 |
ClinGen | rs188698686 |
ebi | rs188698686 |
HLI | rs188698686 |
Exac | rs188698686 |
Gnomad | rs188698686 |
Varsome | rs188698686 |
LitVar | rs188698686 |
Map | rs188698686 |
PheGenI | rs188698686 |
Biobank | rs188698686 |
1000 genomes | rs188698686 |
hgdp | rs188698686 |
ensembl | rs188698686 |
geneview | rs188698686 |
scholar | rs188698686 |
rs188698686 | |
pharmgkb | rs188698686 |
gwascentral | rs188698686 |
openSNP | rs188698686 |
23andMe | rs188698686 |
SNPshot | rs188698686 |
SNPdbe | rs188698686 |
MSV3d | rs188698686 |
GWAS Ctlg | rs188698686 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs188698686(G;G) |
Alt | rs188698686(G;G) |
Reference | Rs188698686(A;A) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | SLC22A5 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000005.9:g.131721061A>C |
CLNSRC | |
CLNACC | RCV000186138.1, |