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- Data Summary
SNP Report
Basic Info
| Name | rs239915 dbSNP Ensembl | ||
|---|---|---|---|
| Location | Chr22:22316631(Fwd) | ||
| Variant Alleles | G/A | ||
| Ancestral Allele | G | ||
| Functional Annotation | 3_prime_UTR_variant; NMD_transcript_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant. | ||
| Consequence to Transcript | 3_prime_UTR_variant(ENST00000413067) NMD_transcript_variant(ENST00000436282; ENST00000444502; ENST00000457179) intron_variant(ENST00000457270; ENST00000398793; ENST00000436282; ENST00000444502; ENST00000457179; ENST00000357179) nc_transcript_variant(ENST00000470338) non_coding_exon_variant(ENST00000470338) |
||
| 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.