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- Data Summary
SNP Report
Basic Info
| Name | rs4938016 dbSNP Ensembl | ||
|---|---|---|---|
| Location | chr11:113270015(Fwd) | ||
| Variant Alleles | G/C/T | ||
| Ancestral Allele | C | ||
| Functional Annotation | downstream_gene_variant; missense_variant.
Polyphen Annotation: benign(ENST00000303941) SIFT Annotation: tolerated(ENST00000303941) |
||
| Consequence to Transcript | downstream_gene_variant(ENST00000542948) missense_variant(ENST00000303941) |
||
| No. of Studies | 0 (significant: 0; non-significant: 0; trend: 0) | ||
| Source | LD-proxy | ||
SNP related studies (count: 0)
SNP related genes (count: 1)
