SNP Report
Name | rs4659395 dbSNP Ensembl | ||
---|---|---|---|
Location | 1:25891774 - 25891774(+) | ||
Variant Seq | G | ||
Ancestral Allele | A | ||
Ref Seq | A | ||
Minor Allele Frequence | 0.0147764 | ||
Annotation | downstream_gene_variant; intron_variant; non_coding_transcript_variant | ||
Variant Effect | downstream_gene_variant(ENST00000440710, ENST00000453780); intron_variant(ENST00000426559, ENST00000513116); non_coding_transcript_variant(ENST00000513116) | ||
SIFT Annotation | tolerated_-_low_confidence | ||
SIFT Variant Effect | tolerated_-_low_confidence(ENST00000426559) | ||
PolyPhen Annotation | benign | ||
PolyPhen Variant Effect | benign(ENST00000426559) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | Chromatin interactive region | ||
Chromatin State | Enhancers;Weak transcription;Strong transcription;Flanking Active TSS;Genic enhancers | ||
No. of Marker's Association Results | 1 (Positive: 0; Negative: 1; 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.