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- Data Summary
SNP Report
Basic Info
| Name | rs9619267 dbSNP Ensembl | ||
|---|---|---|---|
| Location | Chr22:32886177(Fwd) | ||
| Variant Alleles | C/T | ||
| Ancestral Allele | C | ||
| Functional Annotation | NMD_transcript_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant. | ||
| Consequence to Transcript | NMD_transcript_variant(ENST00000425028; ENST00000420700) intron_variant(ENST00000266087; ENST00000484607; ENST00000382058; ENST00000397426; ENST00000425028; ENST00000420700) nc_transcript_variant(ENST00000484607; ENST00000492535) non_coding_exon_variant(ENST00000492535) |
||
| No. of Studies | 0 (significant: 0; non-significant: 0; trend: 0) | ||
| Source | LD-proxy | ||
SNP related studies (count: 0)
SNP related genes (count: 1)
Literature-origin genes (count: 0)
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.