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- Data Summary
SNP Report
Name | rs13436644 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr5:36608101(Fwd) | ||
Variant Alleles | T/C | ||
Ancestral Allele | T | ||
Functional Annotation | intron_variant; nc_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | intron_variant(ENST00000512374; ENST00000416645; ENST00000505202; ENST00000513903; ENST00000504121; ENST00000265113; ENST00000506725; ENST00000427100) nc_transcript_variant(ENST00000512374; ENST00000504121; ENST00000506725) upstream_gene_variant(ENST00000502864; ENST00000514563; ENST00000513646; ENST00000381918) |
||
No. of Studies | 0 (significant: 0; non-significant: 0; trend: 0) | ||
Source | LD-proxy |
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2>=0.8.