rs370376334
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs370376334(C;C) |
Make rs370376334(C;G) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 2 |
Position | 25244599 |
Gene | DNMT3A |
is a | snp |
is | mentioned by |
dbSNP | rs370376334 |
dbSNP (classic) | rs370376334 |
ClinGen | rs370376334 |
ebi | rs370376334 |
HLI | rs370376334 |
Exac | rs370376334 |
Gnomad | rs370376334 |
Varsome | rs370376334 |
LitVar | rs370376334 |
Map | rs370376334 |
PheGenI | rs370376334 |
Biobank | rs370376334 |
1000 genomes | rs370376334 |
hgdp | rs370376334 |
ensembl | rs370376334 |
geneview | rs370376334 |
scholar | rs370376334 |
rs370376334 | |
pharmgkb | rs370376334 |
gwascentral | rs370376334 |
openSNP | rs370376334 |
23andMe | rs370376334 |
SNPshot | rs370376334 |
SNPdbe | rs370376334 |
MSV3d | rs370376334 |
GWAS Ctlg | rs370376334 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs370376334(C;C) |
Alt | rs370376334(C;C) |
Reference | Rs370376334(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | DNMT3A |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000002.11:g.25467468G>C |
CLNSRC | |
CLNACC | RCV000304967.1, |