SNP Report
Name | rs17244296 dbSNP Ensembl | ||
---|---|---|---|
Location | 11:28074556 - 28074556(+) | ||
Variant Seq | T | ||
Ancestral Allele | A | ||
Ref Seq | A | ||
Minor Allele Frequence | 0.386581 | ||
Annotation | downstream_gene_variant; intron_variant | ||
Variant Effect | downstream_gene_variant(ENST00000533466); intron_variant(ENST00000263181) | ||
SIFT Annotation | tolerated | ||
SIFT Variant Effect | tolerated(ENST00000263181) | ||
PolyPhen Annotation | possibly_damaging | ||
PolyPhen Variant Effect | possibly_damaging(ENST00000263181) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | n/a | ||
Chromatin State | Weak transcription;Strong transcription;Active TSS | ||
No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |