rs141957107
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs141957107(C;T) |
Make rs141957107(T;T) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 2 |
Position | 227688165 |
Gene | SLC19A3 |
is a | snp |
is | mentioned by |
dbSNP | rs141957107 |
dbSNP (classic) | rs141957107 |
ClinGen | rs141957107 |
ebi | rs141957107 |
HLI | rs141957107 |
Exac | rs141957107 |
Gnomad | rs141957107 |
Varsome | rs141957107 |
LitVar | rs141957107 |
Map | rs141957107 |
PheGenI | rs141957107 |
Biobank | rs141957107 |
1000 genomes | rs141957107 |
hgdp | rs141957107 |
ensembl | rs141957107 |
geneview | rs141957107 |
scholar | rs141957107 |
rs141957107 | |
pharmgkb | rs141957107 |
gwascentral | rs141957107 |
openSNP | rs141957107 |
23andMe | rs141957107 |
SNPshot | rs141957107 |
SNPdbe | rs141957107 |
MSV3d | rs141957107 |
GWAS Ctlg | rs141957107 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs141957107(T;T) |
Alt | rs141957107(T;T) |
Reference | Rs141957107(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | SLC19A3 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000002.11:g.228552881C>T |
CLNSRC | |
CLNACC | RCV000255502.1, |