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- Data Summary
SNP Report
Name | rs2042449 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr5:1416646(Fwd) | ||
Variant Alleles | G/A | ||
Ancestral Allele | G | ||
Functional Annotation | intron_variant; nc_transcript_variant; non_coding_exon_variant. | ||
Consequence to Transcript | intron_variant(ENST00000453492; ENST00000513308; ENST00000270349) nc_transcript_variant(ENST00000511750) non_coding_exon_variant(ENST00000511750) |
||
No. of Studies | 2 (significant: 1; 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.