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- Data Summary
SNP Report
Name | rs9534495 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr13:47429228(Fwd) | ||
Variant Alleles | A/G | ||
Ancestral Allele | A | ||
Functional Annotation | downstream_gene_variant; intron_variant; nc_transcript_variant. | ||
Consequence to Transcript | downstream_gene_variant(ENST00000452352) intron_variant(ENST00000455126; ENST00000430913; ENST00000542664; ENST00000543956; ENST00000378688) nc_transcript_variant(ENST00000455126; ENST00000430913) |
||
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.