rs142553916
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs142553916(A;A) |
Make rs142553916(A;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 6 |
Position | 73621883 |
Gene | SLC17A5 |
is a | snp |
is | mentioned by |
dbSNP | rs142553916 |
dbSNP (classic) | rs142553916 |
ClinGen | rs142553916 |
ebi | rs142553916 |
HLI | rs142553916 |
Exac | rs142553916 |
Gnomad | rs142553916 |
Varsome | rs142553916 |
LitVar | rs142553916 |
Map | rs142553916 |
PheGenI | rs142553916 |
Biobank | rs142553916 |
1000 genomes | rs142553916 |
hgdp | rs142553916 |
ensembl | rs142553916 |
geneview | rs142553916 |
scholar | rs142553916 |
rs142553916 | |
pharmgkb | rs142553916 |
gwascentral | rs142553916 |
openSNP | rs142553916 |
23andMe | rs142553916 |
SNPshot | rs142553916 |
SNPdbe | rs142553916 |
MSV3d | rs142553916 |
GWAS Ctlg | rs142553916 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs142553916(A;A) |
Alt | rs142553916(A;A) |
Reference | Rs142553916(G;G) |
Significance | Other |
Disease | not provided |
Variation | info |
Gene | SLC17A5 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000006.11:g.74331606G>A |
CLNSRC | |
CLNACC | RCV000171400.2, |