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- Data Summary
SNP Report
Name | rs2601126 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr3:11036624(Fwd) | ||
Variant Alleles | C/T | ||
Ancestral Allele | T | ||
Functional Annotation | intron_variant; nc_transcript_variant. | ||
Consequence to Transcript | intron_variant(ENST00000287766; ENST00000425938; ENST00000462473) nc_transcript_variant(ENST00000462473) |
||
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.