SNP Report
| Name | rs6602398 dbSNP Ensembl | ||
|---|---|---|---|
| Location | 10:6040990 - 6040990(+) | ||
| Variant Seq | T | ||
| Ancestral Allele | G | ||
| Ref Seq | G | ||
| Minor Allele Frequence | 0.161342 | ||
| Annotation | downstream_gene_variant; intron_variant | ||
| Variant Effect | downstream_gene_variant(ENST00000440436); intron_variant(ENST00000379954, LRG_73t1, ENST00000256876, ENST00000379959) | ||
| SIFT Annotation | deleterious | ||
| SIFT Variant Effect | deleterious(LRG_73t1, ENST00000447847, ENST00000379959, ENST00000379954, ENST00000256876) | ||
| PolyPhen Annotation | probably_damaging | ||
| PolyPhen Variant Effect | probably_damaging(LRG_73t1, ENST00000447847, ENST00000379959, ENST00000379954, ENST00000256876) | ||
| rSNP? | Yes Link in rVarBase | ||
| Related Regulatory Elements | n/a | ||
| Chromatin State | Weak transcription;Enhancers;Genic enhancers | ||
| 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.



