rs748082838
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs748082838(C;T) |
Make rs748082838(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 2 |
Position | 25244258 |
Gene | DNMT3A |
is a | snp |
is | mentioned by |
dbSNP | rs748082838 |
dbSNP (classic) | rs748082838 |
ClinGen | rs748082838 |
ebi | rs748082838 |
HLI | rs748082838 |
Exac | rs748082838 |
Gnomad | rs748082838 |
Varsome | rs748082838 |
LitVar | rs748082838 |
Map | rs748082838 |
PheGenI | rs748082838 |
Biobank | rs748082838 |
1000 genomes | rs748082838 |
hgdp | rs748082838 |
ensembl | rs748082838 |
geneview | rs748082838 |
scholar | rs748082838 |
rs748082838 | |
pharmgkb | rs748082838 |
gwascentral | rs748082838 |
openSNP | rs748082838 |
23andMe | rs748082838 |
SNPshot | rs748082838 |
SNPdbe | rs748082838 |
MSV3d | rs748082838 |
GWAS Ctlg | rs748082838 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs748082838(T;T) |
Alt | rs748082838(T;T) |
Reference | Rs748082838(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | DNMT3A |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000002.11:g.25467127C>T |
CLNSRC | |
CLNACC | RCV000483070.1, |