SNP Report
| Name | rs2073836 dbSNP Ensembl | ||
|---|---|---|---|
| Location | 9:133667012 - 133667012(+) | ||
| Variant Seq | T | ||
| Ancestral Allele | T | ||
| Ref Seq | A | ||
| Minor Allele Frequence | 0.368411 | ||
| Annotation | non_coding_transcript_exon_variant; intron_variant; non_coding_transcript_variant | ||
| Variant Effect | non_coding_transcript_exon_variant(ENST00000469828); intron_variant(ENST00000371872, ENST00000439388, ENST00000371868, ENST00000422262); non_coding_transcript_variant(ENST00000469828) | ||
| SIFT Annotation | deleterious | ||
| SIFT Variant Effect | deleterious(ENST00000393056) | ||
| PolyPhen Annotation | probably_damaging | ||
| PolyPhen Variant Effect | probably_damaging(ENST00000393056) | ||
| rSNP? | Yes Link in rVarBase | ||
| Related Regulatory Elements | lncRNA | ||
| Chromatin State | Weak transcription;Genic enhancers;Enhancers;Strong transcription;Bivalent Enhancer | ||
| No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
| Source | LD-proxy | ||


