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- Data Summary
SNP Report
Name | rs591556 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr11:18061400(Fwd) | ||
Variant Alleles | T/C | ||
Ancestral Allele | T | ||
Functional Annotation | NMD_transcript_variant; intron_variant. | ||
Consequence to Transcript | NMD_transcript_variant(ENST00000417164) intron_variant(ENST00000250018; ENST00000341556; ENST00000417164; ENST00000528338) |
||
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.