SNP Report
Name | rs2071532 dbSNP Ensembl | ||
---|---|---|---|
Location | 11:18044198 - 18044198(+) | ||
Variant Seq | T | ||
Ancestral Allele | C | ||
Ref Seq | C | ||
Minor Allele Frequence | 0.498403 | ||
Annotation | upstream_gene_variant | ||
Variant Effect | upstream_gene_variant(ENST00000250018, ENST00000528338, ENST00000417164) | ||
SIFT Annotation | deleterious_-_low_confidence; deleterious | ||
SIFT Variant Effect | deleterious_-_low_confidence(ENST00000417164, ENST00000250018); deleterious(ENST00000528338) | ||
PolyPhen Annotation | benign; possibly_damaging | ||
PolyPhen Variant Effect | benign(ENST00000528338); possibly_damaging(ENST00000417164, ENST00000250018) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | n/a | ||
Chromatin State | Weak transcription | ||
No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |