rs767226511
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs767226511(A;A) |
Make rs767226511(A;C) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 2 |
Position | 25244579 |
Gene | DNMT3A |
is a | snp |
is | mentioned by |
dbSNP | rs767226511 |
dbSNP (classic) | rs767226511 |
ClinGen | rs767226511 |
ebi | rs767226511 |
HLI | rs767226511 |
Exac | rs767226511 |
Gnomad | rs767226511 |
Varsome | rs767226511 |
LitVar | rs767226511 |
Map | rs767226511 |
PheGenI | rs767226511 |
Biobank | rs767226511 |
1000 genomes | rs767226511 |
hgdp | rs767226511 |
ensembl | rs767226511 |
geneview | rs767226511 |
scholar | rs767226511 |
rs767226511 | |
pharmgkb | rs767226511 |
gwascentral | rs767226511 |
openSNP | rs767226511 |
23andMe | rs767226511 |
SNPshot | rs767226511 |
SNPdbe | rs767226511 |
MSV3d | rs767226511 |
GWAS Ctlg | rs767226511 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs767226511(A;A) rs767226511(G;G) rs767226511(T;T) |
Alt | rs767226511(A;A) rs767226511(G;G) rs767226511(T;T) |
Reference | Rs767226511(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | DNMT3A |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000002.11:g.25467448C>T |
CLNSRC | |
CLNACC | RCV000486870.1, |