SNP Report
| Name | rs16942660 dbSNP Ensembl | ||
|---|---|---|---|
| Location | 15:60508867 - 60508867(+) | ||
| Variant Seq | T | ||
| Ancestral Allele | C | ||
| Ref Seq | C | ||
| Minor Allele Frequence | 0.0341454 | ||
| Annotation | downstream_gene_variant; upstream_gene_variant; intron_variant; non_coding_transcript_variant | ||
| Variant Effect | downstream_gene_variant(ENST00000559343, ENST00000551975, ENST00000560004); upstream_gene_variant(ENST00000559902); intron_variant(ENST00000501579, ENST00000558235, ENST00000335670, ENST00000261523, ENST00000449337, ENST00000309157, ENST00000558140, ENST00000559587, ENST00000559824); non_coding_transcript_variant(ENST00000501579, ENST00000558235, ENST00000558140, ENST00000559587, ENST00000559824) | ||
| SIFT Annotation | tolerated | ||
| SIFT Variant Effect | tolerated(ENST00000309157, ENST00000335670, ENST00000449337, ENST00000261523) | ||
| PolyPhen Annotation | benign; possibly_damaging | ||
| PolyPhen Variant Effect | benign(ENST00000335670, ENST00000261523); possibly_damaging(ENST00000309157, ENST00000449337) | ||
| rSNP? | Yes Link in rVarBase | ||
| Related Regulatory Elements | TF binding region;Chromatin interactive region | ||
| Chromatin State | Weak transcription;Enhancers;Strong transcription;Genic enhancers | ||
| No. of Marker's Association Results | 2 (Positive: 1; Negative: 1; 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.



