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SNP Report
| Name | rs3016389 dbSNP Ensembl | ||
|---|---|---|---|
| Location | chr11:132696192 - 132696192(1) | ||
| Variant Alleles | T/C | ||
| Ancestral Allele | T | ||
| Minor Allele | C | ||
| Minor Allele Frequence | 0.486022 | ||
| Functional Annotation | intron_variant; non_coding_transcript_variant. | ||
| Consequence to Transcript | intron_variant(ENST00000331898, ENST00000374778, ENST00000524381, ENST00000525412, ENST00000529038, ENST00000541867, ENST00000612177); non_coding_transcript_variant(ENST00000525412, ENST00000529038) | ||
| No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
| Source | LD-proxy | ||


