SNP Report
Name | rs8036584 dbSNP Ensembl | ||
---|---|---|---|
Location | 15:32114089 - 32114089(+) | ||
Variant Seq | C | ||
Ref Seq | T | ||
Minor Allele Frequence | 0.134585 | ||
Annotation | intron_variant; NMD_transcript_variant | ||
Variant Effect | intron_variant(ENST00000437966, ENST00000454250, ENST00000306901); NMD_transcript_variant(ENST00000437966) | ||
SIFT Annotation | tolerated | ||
SIFT Variant Effect | tolerated(ENST00000306901, ENST00000454250) | ||
PolyPhen Annotation | benign | ||
PolyPhen Variant Effect | benign(ENST00000306901, ENST00000454250) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | n/a | ||
Chromatin State | Weak transcription | ||
No. of Marker's Association Results | 1 (Positive: 1; Negative: 0; Trend: 0) | ||
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.