rs759157320
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs759157320(C;T) |
Make rs759157320(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 17 |
Position | 75278290 |
Gene | SLC25A19 |
is a | snp |
is | mentioned by |
dbSNP | rs759157320 |
dbSNP (classic) | rs759157320 |
ClinGen | rs759157320 |
ebi | rs759157320 |
HLI | rs759157320 |
Exac | rs759157320 |
Gnomad | rs759157320 |
Varsome | rs759157320 |
LitVar | rs759157320 |
Map | rs759157320 |
PheGenI | rs759157320 |
Biobank | rs759157320 |
1000 genomes | rs759157320 |
hgdp | rs759157320 |
ensembl | rs759157320 |
geneview | rs759157320 |
scholar | rs759157320 |
rs759157320 | |
pharmgkb | rs759157320 |
gwascentral | rs759157320 |
openSNP | rs759157320 |
23andMe | rs759157320 |
SNPshot | rs759157320 |
SNPdbe | rs759157320 |
MSV3d | rs759157320 |
GWAS Ctlg | rs759157320 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs759157320(T;T) |
Alt | rs759157320(T;T) |
Reference | Rs759157320(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | SLC25A19 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000017.10:g.73274371C>T |
CLNSRC | |
CLNACC | RCV000171266.1, |