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- Data Summary
SNP Report
Name | rs2397772 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr16:55724477(Fwd) | ||
Variant Alleles | C/G | ||
Ancestral Allele | C | ||
Functional Annotation | intron_variant. | ||
Consequence to Transcript | intron_variant(ENST00000568529; ENST00000379906; ENST00000414754; ENST00000219833; ENST00000566163; ENST00000567238; ENST00000561820; ENST00000568943) | ||
No. of Studies | 0 (significant: 0; non-significant: 0; trend: 0) | ||
Source | LD-proxy |
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2>=0.8.