SNP Report
Name | rs7866350 dbSNP Ensembl | ||
---|---|---|---|
Location | 9:98221544 - 98221544(+) | ||
Variant Seq | G,T | ||
Ancestral Allele | C | ||
Ref Seq | C | ||
Minor Allele Frequence | 0.209065 | ||
Annotation | intron_variant; non_coding_transcript_variant | ||
Variant Effect | intron_variant(ENST00000342112, ENST00000493589, ENST00000375066, ENST00000375064, ENST00000465784); non_coding_transcript_variant(ENST00000493589) | ||
SIFT Annotation | tolerated | ||
SIFT Variant Effect | tolerated(ENST00000375066, ENST00000465784, ENST00000342112, ENST00000375064) | ||
PolyPhen Annotation | benign | ||
PolyPhen Variant Effect | benign(ENST00000375066, ENST00000465784, ENST00000342112, ENST00000375064) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | Chromatin interactive region | ||
Chromatin State | Weak transcription;Strong transcription;Enhancers;Genic enhancers | ||
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.