rs10486275
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10486275(C;C) |
Make rs10486275(C;T) |
Make rs10486275(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 8963946 |
is a | snp |
is | mentioned by |
dbSNP | rs10486275 |
dbSNP (classic) | rs10486275 |
ClinGen | rs10486275 |
ebi | rs10486275 |
HLI | rs10486275 |
Exac | rs10486275 |
Gnomad | rs10486275 |
Varsome | rs10486275 |
LitVar | rs10486275 |
Map | rs10486275 |
PheGenI | rs10486275 |
Biobank | rs10486275 |
1000 genomes | rs10486275 |
hgdp | rs10486275 |
ensembl | rs10486275 |
geneview | rs10486275 |
scholar | rs10486275 |
rs10486275 | |
pharmgkb | rs10486275 |
gwascentral | rs10486275 |
openSNP | rs10486275 |
23andMe | rs10486275 |
SNPshot | rs10486275 |
SNPdbe | rs10486275 |
MSV3d | rs10486275 |
GWAS Ctlg | rs10486275 |
GMAF | 0.2309 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
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