SNP Report
| Name | rs834811 dbSNP Ensembl | ||
|---|---|---|---|
| Location | 7:136199823 - 136199823(+) | ||
| Variant Seq | G | ||
| Ancestral Allele | G | ||
| Ref Seq | A | ||
| Minor Allele Frequence | 0.480831 | ||
| Annotation | intron_variant; non_coding_transcript_variant | ||
| Variant Effect | intron_variant(ENST00000445293, ENST00000435996); non_coding_transcript_variant(ENST00000445293, ENST00000435996) | ||
| SIFT Annotation | deleterious_-_low_confidence; tolerated | ||
| SIFT Variant Effect | deleterious_-_low_confidence(ENST00000435723); tolerated(ENST00000393085) | ||
| PolyPhen Annotation | unknown; probably_damaging | ||
| PolyPhen Variant Effect | unknown(ENST00000435723); probably_damaging(ENST00000393085) | ||
| rSNP? | No Link in rVarBase | ||
| Related Regulatory Elements | n/a | ||
| Chromatin State | Inactive region | ||
| No. of Marker's Association Results | 1 (Positive: 0; Negative: 0; Trend: 1) | ||
| Source | Literature | ||
The LD data used here is based on 1000 Genome Phase I. LD SNP pairs were selected with a threshold r2<=0.8.



