rs2269879
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2269879(C;C) |
Make rs2269879(C;T) |
Make rs2269879(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 19 |
Position | 2194897 |
Gene | DOT1L |
is a | snp |
is | mentioned by |
dbSNP | rs2269879 |
dbSNP (classic) | rs2269879 |
ClinGen | rs2269879 |
ebi | rs2269879 |
HLI | rs2269879 |
Exac | rs2269879 |
Gnomad | rs2269879 |
Varsome | rs2269879 |
LitVar | rs2269879 |
Map | rs2269879 |
PheGenI | rs2269879 |
Biobank | rs2269879 |
1000 genomes | rs2269879 |
hgdp | rs2269879 |
ensembl | rs2269879 |
geneview | rs2269879 |
scholar | rs2269879 |
rs2269879 | |
pharmgkb | rs2269879 |
gwascentral | rs2269879 |
openSNP | rs2269879 |
23andMe | rs2269879 |
SNPshot | rs2269879 |
SNPdbe | rs2269879 |
MSV3d | rs2269879 |
GWAS Ctlg | rs2269879 |
GMAF | 0.197 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
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[PMID 22440088] Effects of genetic variation in H3K79 methylation regulatory genes on clinical blood pressure and blood pressure response to hydrochlorothiazide