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- Data Summary
SNP Report
Name | rs11111 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr5:37814102(Fwd) | ||
Variant Alleles | T/C | ||
Ancestral Allele | T | ||
Functional Annotation | 3_prime_UTR_variant; downstream_gene_variant. | ||
Consequence to Transcript | 3_prime_UTR_variant(ENST00000344622; ENST00000326524) downstream_gene_variant(ENST00000427982; ENST00000502572; ENST00000515058; ENST00000381826; ENST00000510177) |
||
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.