SNP Report
Name | rs3782203 dbSNP Ensembl | ||
---|---|---|---|
Location | 12:117282606 - 117282606(+) | ||
Variant Seq | C | ||
Ancestral Allele | T | ||
Ref Seq | T | ||
Minor Allele Frequence | 0.153754 | ||
Annotation | upstream_gene_variant; intron_variant | ||
Variant Effect | upstream_gene_variant(ENST00000618414); intron_variant(ENST00000344089, ENST00000317775, ENST00000618760, ENST00000338101) | ||
SIFT Annotation | tolerated | ||
SIFT Variant Effect | tolerated(ENST00000344089, ENST00000317775, ENST00000338101, ENST00000618760) | ||
PolyPhen Annotation | benign | ||
PolyPhen Variant Effect | benign(ENST00000344089, ENST00000317775, ENST00000338101, ENST00000618760) | ||
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 |