rs149095705
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs149095705(A;A) |
Make rs149095705(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 2 |
Position | 25234307 |
Gene | DNMT3A |
is a | snp |
is | mentioned by |
dbSNP | rs149095705 |
dbSNP (classic) | rs149095705 |
ClinGen | rs149095705 |
ebi | rs149095705 |
HLI | rs149095705 |
Exac | rs149095705 |
Gnomad | rs149095705 |
Varsome | rs149095705 |
LitVar | rs149095705 |
Map | rs149095705 |
PheGenI | rs149095705 |
Biobank | rs149095705 |
1000 genomes | rs149095705 |
hgdp | rs149095705 |
ensembl | rs149095705 |
geneview | rs149095705 |
scholar | rs149095705 |
rs149095705 | |
pharmgkb | rs149095705 |
gwascentral | rs149095705 |
openSNP | rs149095705 |
23andMe | rs149095705 |
SNPshot | rs149095705 |
SNPdbe | rs149095705 |
MSV3d | rs149095705 |
GWAS Ctlg | rs149095705 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs149095705(A;A) rs149095705(C;C) rs149095705(T;T) |
Alt | rs149095705(A;A) rs149095705(C;C) rs149095705(T;T) |
Reference | Rs149095705(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | DNMT3A |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000002.11:g.25457176G>A |
CLNSRC | |
CLNACC | RCV000413992.1, |