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- Data Summary
SNP Report
Basic Info
| Name | rs7180812 dbSNP Ensembl | ||
|---|---|---|---|
| Location | Chr15:43695231(Fwd) | ||
| Variant Alleles | A/G | ||
| Ancestral Allele | A | ||
| Functional Annotation | NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant. | ||
| Consequence to Transcript | NMD_transcript_variant(ENST00000561691; ENST00000566251) downstream_gene_variant(ENST00000562053; ENST00000263801; ENST00000476454; ENST00000382044; ENST00000382039; ENST00000411772; ENST00000450115) intron_variant(ENST00000260383; ENST00000399460; ENST00000561691; ENST00000564079; ENST00000566251; ENST00000563147; ENST00000565548) nc_transcript_variant(ENST00000563963) non_coding_exon_variant(ENST00000563963) upstream_gene_variant(ENST00000570057) |
||
| No. of Studies | 0 (significant: 0; non-significant: 0; trend: 0) | ||
| Source | LD-proxy | ||
SNP related studies (count: 0)
SNP related genes (count: 2)
Literature-origin genes (count: 0)
Genes from other sources 
(count: 2)
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2>=0.8.