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- Data Summary
SNP Report
Basic Info
| Name | rs16969968 dbSNP Ensembl | ||
|---|---|---|---|
| Location | chr15:78882925(Fwd) | ||
| Variant Alleles | G/A | ||
| Ancestral Allele | G | ||
| Functional Annotation | downstream_gene_variant; intron_variant; missense_variant; nc_transcript_variant; non_coding_exon_variant.
Polyphen Annotation: benign(ENST00000299565) SIFT Annotation: tolerated(ENST00000299565) |
||
| Consequence to Transcript | downstream_gene_variant(ENST00000326828; ENST00000348639; ENST00000559002; ENST00000559658) intron_variant(ENST00000394802; ENST00000559554; ENST00000559576) missense_variant(ENST00000299565) nc_transcript_variant(ENST00000567141) non_coding_exon_variant(ENST00000567141) |
||
| No. of Studies | 0 (significant: 0; non-significant: 0; trend: 0) | ||
| Source | LD-proxy | ||
SNP related studies (count: 0)
SNP related genes (count: 2)
