rs6889665
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6889665(C;C) |
Make rs6889665(C;T) |
Make rs6889665(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 23532534 |
is a | snp |
is | mentioned by |
dbSNP | rs6889665 |
dbSNP (classic) | rs6889665 |
ClinGen | rs6889665 |
ebi | rs6889665 |
HLI | rs6889665 |
Exac | rs6889665 |
Gnomad | rs6889665 |
Varsome | rs6889665 |
LitVar | rs6889665 |
Map | rs6889665 |
PheGenI | rs6889665 |
Biobank | rs6889665 |
1000 genomes | rs6889665 |
hgdp | rs6889665 |
ensembl | rs6889665 |
geneview | rs6889665 |
scholar | rs6889665 |
rs6889665 | |
pharmgkb | rs6889665 |
gwascentral | rs6889665 |
openSNP | rs6889665 |
23andMe | rs6889665 |
SNPshot | rs6889665 |
SNPdbe | rs6889665 |
MSV3d | rs6889665 |
GWAS Ctlg | rs6889665 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
rs6889665 near a 17-base-pair DNA sequence associated with crossover targets in people of West African ancestry. [PMID 21775986]