rs9786099
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs9786099(C;C) |
Make rs9786099(C;T) |
Make rs9786099(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | Y |
Position | 21079682 |
is a | snp |
is | mentioned by |
dbSNP | rs9786099 |
dbSNP (classic) | rs9786099 |
ClinGen | rs9786099 |
ebi | rs9786099 |
HLI | rs9786099 |
Exac | rs9786099 |
Gnomad | rs9786099 |
Varsome | rs9786099 |
LitVar | rs9786099 |
Map | rs9786099 |
PheGenI | rs9786099 |
Biobank | rs9786099 |
1000 genomes | rs9786099 |
hgdp | rs9786099 |
ensembl | rs9786099 |
geneview | rs9786099 |
scholar | rs9786099 |
rs9786099 | |
pharmgkb | rs9786099 |
gwascentral | rs9786099 |
openSNP | rs9786099 |
23andMe | rs9786099 |
SNPshot | rs9786099 |
SNPdbe | rs9786099 |
MSV3d | rs9786099 |
GWAS Ctlg | rs9786099 |
Y Chrom | rs9786099 |
GMAF | 0.1653 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
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