rs879253953
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(CGAG;CGAG) | 0 | common in clinvar |
Make rs879253953(-;-) |
Make rs879253953(-;CGAG) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 19 |
Position | 10154672 |
Gene | DNMT1 |
is a | snp |
is | mentioned by |
dbSNP | rs879253953 |
dbSNP (classic) | rs879253953 |
ClinGen | rs879253953 |
ebi | rs879253953 |
HLI | rs879253953 |
Exac | rs879253953 |
Gnomad | rs879253953 |
Varsome | rs879253953 |
LitVar | rs879253953 |
Map | rs879253953 |
PheGenI | rs879253953 |
Biobank | rs879253953 |
1000 genomes | rs879253953 |
hgdp | rs879253953 |
ensembl | rs879253953 |
geneview | rs879253953 |
scholar | rs879253953 |
rs879253953 | |
pharmgkb | rs879253953 |
gwascentral | rs879253953 |
openSNP | rs879253953 |
23andMe | rs879253953 |
SNPshot | rs879253953 |
SNPdbe | rs879253953 |
MSV3d | rs879253953 |
GWAS Ctlg | rs879253953 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs879253953(-;-) |
Alt | rs879253953(-;-) |
Reference | Rs879253953(CGAG;CGAG) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | DNMT1 |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000019.9:g.10265348_10265351delCTCG |
CLNSRC | |
CLNACC | RCV000235546.1, |