SNP Report
Basic Info
| Name | rs11177067 dbSNP Ensembl | ||
|---|---|---|---|
| Location | 12:68133107 - 68133107(+) | ||
| Variant Seq | C | ||
| Ancestral Allele | T | ||
| Ref Seq | T | ||
| Minor Allele Frequence | 0.123203 | ||
| Annotation | intron_variant; non_coding_transcript_variant | ||
| Variant Effect | intron_variant(ENST00000536914); non_coding_transcript_variant(ENST00000536914) | ||
| SIFT Annotation | tolerated | ||
| SIFT Variant Effect | tolerated(ENST00000393555, ENST00000344096) | ||
| PolyPhen Annotation | benign | ||
| PolyPhen Variant Effect | benign(ENST00000393555, ENST00000344096) | ||
| rSNP? | Yes Link in rVarBase | ||
| Related Regulatory Elements | n/a | ||
| Chromatin State | Enhancers;Weak transcription | ||
| No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
| Source | LD-proxy | ||
SNP related association results
SNP related genes (count: 1)
| Approved Symbol | Approved Name | Location | No. of Association Results (Positive/Negative/Trend)  |
|---|---|---|---|
| IFNG-AS1 | IFNG antisense RNA 1 | 12q15 | Mapped by Literature SNP, Mapped by LD-proxy |
SNPs in LD with rs11177067 (count: 0)
SNP related eQTL (count: 1)