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- Data Summary
SNP Report
Name | rs1150222 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr11:113846872(Fwd) | ||
Variant Alleles | G/T | ||
Ancestral Allele | G | ||
Functional Annotation | NMD_transcript_variant; intron_variant; upstream_gene_variant. | ||
Consequence to Transcript | NMD_transcript_variant(ENST00000510849) intron_variant(ENST00000355556; ENST00000504030; ENST00000375498; ENST00000535865; ENST00000510849; ENST00000506841) upstream_gene_variant(ENST00000502622; ENST00000299961) |
||
No. of Studies | 1 (significant: 1; non-significant: 0; 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.