rs779626155
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs779626155(A;A) |
Make rs779626155(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 2 |
Position | 25240313 |
Gene | DNMT3A |
is a | snp |
is | mentioned by |
dbSNP | rs779626155 |
dbSNP (classic) | rs779626155 |
ClinGen | rs779626155 |
ebi | rs779626155 |
HLI | rs779626155 |
Exac | rs779626155 |
Gnomad | rs779626155 |
Varsome | rs779626155 |
LitVar | rs779626155 |
Map | rs779626155 |
PheGenI | rs779626155 |
Biobank | rs779626155 |
1000 genomes | rs779626155 |
hgdp | rs779626155 |
ensembl | rs779626155 |
geneview | rs779626155 |
scholar | rs779626155 |
rs779626155 | |
pharmgkb | rs779626155 |
gwascentral | rs779626155 |
openSNP | rs779626155 |
23andMe | rs779626155 |
SNPshot | rs779626155 |
SNPdbe | rs779626155 |
MSV3d | rs779626155 |
GWAS Ctlg | rs779626155 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs779626155(A;A) |
Alt | rs779626155(A;A) |
Reference | Rs779626155(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | DNMT3A |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000002.11:g.25463182G>A |
CLNSRC | |
CLNACC | RCV000486209.1, |