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- Data Summary
SNP Report
Name | rs1555322 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr20:33849179(Fwd) | ||
Variant Alleles | G/A | ||
Ancestral Allele | G | ||
Functional Annotation | intron_variant; nc_transcript_variant. | ||
Consequence to Transcript | intron_variant(ENST00000453892; ENST00000438751; ENST00000566203; ENST00000540582; ENST00000454184; ENST00000246186; ENST00000433764; ENST00000456350) nc_transcript_variant(ENST00000453892; ENST00000438751; ENST00000566203; ENST00000454184; ENST00000456350; ENST00000433764) |
||
No. of Studies | 1 (significant: 0; non-significant: 0; trend: 1) | ||
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.