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- Data Summary
SNP Report
Name | rs1157690 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr8:26610152(Fwd) | ||
Variant Alleles | C/T | ||
Ancestral Allele | C | ||
Functional Annotation | NMD_transcript_variant; downstream_gene_variant; intron_variant. | ||
Consequence to Transcript | NMD_transcript_variant(ENST00000519096) downstream_gene_variant(ENST00000521711; ENST00000380582; ENST00000519229; ENST00000380581) intron_variant(ENST00000380586; ENST00000519096; ENST00000380587) |
||
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.