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- Data Summary
SNP Report
Name | rs6039769 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr20:10198954(Fwd) | ||
Variant Alleles | A/C | ||
Ancestral Allele | C | ||
Functional Annotation | intron_variant; nc_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | intron_variant(ENST00000453544; ENST00000426491; ENST00000421143; ENST00000451151) nc_transcript_variant(ENST00000453544; ENST00000426491; ENST00000421143; ENST00000451151) upstream_gene_variant(ENST00000304886; ENST00000254976; ENST00000430336) |
||
No. of Studies | 1 (significant: 0; non-significant: 1; 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.