rs745714537
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs745714537(A;C) |
Make rs745714537(C;C) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 2 |
Position | 25240411 |
Gene | DNMT3A |
is a | snp |
is | mentioned by |
dbSNP | rs745714537 |
dbSNP (classic) | rs745714537 |
ClinGen | rs745714537 |
ebi | rs745714537 |
HLI | rs745714537 |
Exac | rs745714537 |
Gnomad | rs745714537 |
Varsome | rs745714537 |
LitVar | rs745714537 |
Map | rs745714537 |
PheGenI | rs745714537 |
Biobank | rs745714537 |
1000 genomes | rs745714537 |
hgdp | rs745714537 |
ensembl | rs745714537 |
geneview | rs745714537 |
scholar | rs745714537 |
rs745714537 | |
pharmgkb | rs745714537 |
gwascentral | rs745714537 |
openSNP | rs745714537 |
23andMe | rs745714537 |
SNPshot | rs745714537 |
SNPdbe | rs745714537 |
MSV3d | rs745714537 |
GWAS Ctlg | rs745714537 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs745714537(C;C) rs745714537(T;T) |
Alt | rs745714537(C;C) rs745714537(T;T) |
Reference | Rs745714537(A;A) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | DNMT3A |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000002.11:g.25463280A>C |
CLNSRC | |
CLNACC | RCV000422670.1, |