SNP Report
Name | rs17115439 dbSNP Ensembl | ||
---|---|---|---|
Location | 11:113393550 - 113393550(+) | ||
Variant Seq | C | ||
Ancestral Allele | C | ||
Ref Seq | T | ||
Minor Allele Frequence | 0.474042 | ||
Annotation | synonymous_variant; upstream_gene_variant | ||
Variant Effect | synonymous_variant(ENST00000303941); upstream_gene_variant(ENST00000542948) | ||
SIFT Annotation | deleterious; tolerated | ||
SIFT Variant Effect | deleterious(ENST00000303941, ENST00000542948); tolerated(ENST00000303941) | ||
PolyPhen Annotation | benign; possibly_damaging | ||
PolyPhen Variant Effect | benign(ENST00000303941, ENST00000542948); possibly_damaging(ENST00000303941) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | n/a | ||
Chromatin State | Weak transcription;Strong transcription;Enhancers | ||
No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |