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- Data Summary
SNP Report
Basic Info
| Name | rs17110424 dbSNP Ensembl | ||
|---|---|---|---|
| Location | Chr12:72314791(Fwd) | ||
| Variant Alleles | A/G | ||
| Ancestral Allele | A | ||
| Functional Annotation | NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant. | ||
| Consequence to Transcript | NMD_transcript_variant(ENST00000462788) downstream_gene_variant(ENST00000483828; ENST00000548679) intron_variant(ENST00000550746; ENST00000319106; ENST00000462788; ENST00000485960; ENST00000393309; ENST00000546450) nc_transcript_variant(ENST00000546450) |
||
| 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.