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- Data Summary
SNP Report
Name | rs10521329 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr16:55720458(Fwd) | ||
Variant Alleles | C/A | ||
Ancestral Allele | C | ||
Functional Annotation | intron_variant. | ||
Consequence to Transcript | intron_variant(ENST00000379906; ENST00000568529; ENST00000414754; ENST00000219833; ENST00000566163; ENST00000561820; ENST00000568943; ENST00000567238) | ||
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.