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- Data Summary
SNP Report
Basic Info
| Name | rs7778762 dbSNP Ensembl | ||
|---|---|---|---|
| Location | Chr7:73110832(Fwd) | ||
| Variant Alleles | C/T | ||
| Ancestral Allele | T | ||
| Functional Annotation | 3_prime_UTR_variant; NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant. | ||
| Consequence to Transcript | 3_prime_UTR_variant(ENST00000421744) NMD_transcript_variant(ENST00000430270; ENST00000436944; ENST00000430446; ENST00000421744) downstream_gene_variant(ENST00000497980; ENST00000491427; ENST00000496216; ENST00000395155; ENST00000441822; ENST00000428163; ENST00000487006; ENST00000222812; ENST00000395156; ENST00000484736; ENST00000480126; ENST00000491645; ENST00000395154; ENST00000478670; ENST00000432522; ENST00000496153) intron_variant(ENST00000463307; ENST00000430270; ENST00000423497; ENST00000436944; ENST00000430446; ENST00000442099; ENST00000453316; ENST00000423166; ENST00000265758) nc_transcript_variant(ENST00000463307; ENST00000471215) non_coding_exon_variant(ENST00000471215) |
||
| 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.