SNP Report
Basic Info
| Name | rs74099930 dbSNP Ensembl | ||
|---|---|---|---|
| Location | 12:68143492 - 68143492(+) | ||
| Variant Seq | A | ||
| Ancestral Allele | G | ||
| Ref Seq | G | ||
| Minor Allele Frequence | 0.168131 | ||
| Annotation | non_coding_transcript_exon_variant; intron_variant; non_coding_transcript_variant | ||
| Variant Effect | non_coding_transcript_exon_variant(ENST00000542812); intron_variant(ENST00000536914); non_coding_transcript_variant(ENST00000536914, ENST00000542812) | ||
| 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 | lncRNA | ||
| Chromatin State | 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 rs74099930 (count: 0)
SNP related eQTL (count: 1)