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- Data Summary
SNP Report
Name | rs11221064 dbSNP Ensembl |
---|---|
Location | Chr11:127687313(Fwd) |
Variant Alleles | G/C |
Ancestral Allele | G |
No. of Studies | 2 (significant: 0; non-significant: 2; trend: 0) |
Source | Literature-origin |
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2>=0.8.