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- Data Summary
SNP Report
Basic Info
| Name | rs351771 dbSNP Ensembl | ||
|---|---|---|---|
| Location | Chr5:112164561(Fwd) | ||
| Variant Alleles | G/A | ||
| Ancestral Allele | A | ||
| Functional Annotation | 3_prime_UTR_variant; NMD_transcript_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant; synonymous_variant. | ||
| Consequence to Transcript | 3_prime_UTR_variant(ENST00000508624) NMD_transcript_variant(ENST00000508624; ENST00000520401) intron_variant(ENST00000502371) nc_transcript_variant(ENST00000504915; ENST00000505084; ENST00000502371; ENST00000514164) non_coding_exon_variant(ENST00000504915; ENST00000505084; ENST00000514164) synonymous_variant(ENST00000507379; ENST00000257430; ENST00000457016; ENST00000508376; ENST00000512211; ENST00000520401; LRG_130_t2; LRG_130_t3; LRG_130_t1) |
||
| 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.