rs77275268
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in complete genomics |
Make rs77275268(C;T) |
Make rs77275268(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 151648063 |
is a | snp |
is | mentioned by |
dbSNP | rs77275268 |
dbSNP (classic) | rs77275268 |
ClinGen | rs77275268 |
ebi | rs77275268 |
HLI | rs77275268 |
Exac | rs77275268 |
Gnomad | rs77275268 |
Varsome | rs77275268 |
LitVar | rs77275268 |
Map | rs77275268 |
PheGenI | rs77275268 |
Biobank | rs77275268 |
1000 genomes | rs77275268 |
hgdp | rs77275268 |
ensembl | rs77275268 |
geneview | rs77275268 |
scholar | rs77275268 |
rs77275268 | |
pharmgkb | rs77275268 |
gwascentral | rs77275268 |
openSNP | rs77275268 |
23andMe | rs77275268 |
SNPshot | rs77275268 |
SNPdbe | rs77275268 |
MSV3d | rs77275268 |
GWAS Ctlg | rs77275268 |
GMAF | 0.1166 |
Max Magnitude | 0 |
[PMID 20661439] Ancestry-Shift Refinement Mapping of the C6orf97-ESR1 Breast Cancer Susceptibility Locus