SNP Report
| Name | rs2108977 dbSNP Ensembl | ||
|---|---|---|---|
| Location | 11:18019049 - 18019049(+) | ||
| Variant Seq | C | ||
| Ref Seq | T | ||
| Minor Allele Frequence | 0.437101 | ||
| Annotation | downstream_gene_variant; 3_prime_UTR_variant; intron_variant; non_coding_transcript_variant | ||
| Variant Effect | downstream_gene_variant(ENST00000417164, ENST00000525406); 3_prime_UTR_variant(ENST00000250018); intron_variant(ENST00000525523); non_coding_transcript_variant(ENST00000525523) | ||
| SIFT Annotation | tolerated | ||
| SIFT Variant Effect | tolerated(ENST00000250018) | ||
| PolyPhen Annotation | possibly_damaging | ||
| PolyPhen Variant Effect | possibly_damaging(ENST00000250018) | ||
| rSNP? | Yes Link in rVarBase | ||
| Related Regulatory Elements | Chromatin interactive region | ||
| Chromatin State | Weak transcription | ||
| No. of Marker's Association Results | 1 (Positive: 1; Negative: 0; Trend: 0) | ||
| Source | Literature | ||
The LD data used here is based on 1000 Genome Phase I. LD SNP pairs were selected with a threshold r2<=0.8.



