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SNP Report
| Name | rs2276266 dbSNP Ensembl | ||
|---|---|---|---|
| Location | chr11:134139965 - 134139965(1) | ||
| Variant Alleles | T/C | ||
| Ancestral Allele | T | ||
| Minor Allele | C | ||
| Minor Allele Frequence | 0.154153 | ||
| Functional Annotation | intron_variant; NMD_transcript_variant; non_coding_transcript_variant. | ||
| Consequence to Transcript | intron_variant(ENST00000299106, ENST00000441717, ENST00000524969, ENST00000531302, ENST00000532165, ENST00000532252, ENST00000534549); NMD_transcript_variant(ENST00000532252); non_coding_transcript_variant(ENST00000524969, ENST00000531302, ENST00000532165) | ||
| No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
| Source | LD-proxy | ||


