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- Data Summary
SNP Report
Basic Info
| Name | rs324376 dbSNP Ensembl | ||
|---|---|---|---|
| Location | Chr7:34756239(Fwd) | ||
| Variant Alleles | T/C | ||
| Ancestral Allele | C | ||
| Functional Annotation | NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant. | ||
| Consequence to Transcript | NMD_transcript_variant(ENST00000381544; ENST00000396095) downstream_gene_variant(ENST00000436945; ENST00000442669) intron_variant(ENST00000419766; ENST00000439852; ENST00000358772; ENST00000539747; ENST00000431669; ENST00000428922; ENST00000537560; ENST00000381542; ENST00000381544; ENST00000535640; ENST00000544556; ENST00000396095; ENST00000531252; ENST00000360581; ENST00000381553; ENST00000359791; ENST00000381539) nc_transcript_variant(ENST00000419766; ENST00000439852; ENST00000358772; ENST00000539747; ENST00000431669; ENST00000428922; ENST00000537560; ENST00000535640; ENST00000544556) |
||
| 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: 1)
Genes from other sources 
(count: 1)
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2>=0.8.