SNP Report
Name | rs2766581 dbSNP Ensembl | ||
---|---|---|---|
Location | 6:35782522 - 35782522(+) | ||
Variant Seq | G | ||
Ancestral Allele | A | ||
Ref Seq | A | ||
Minor Allele Frequence | 0.249201 | ||
Annotation | downstream_gene_variant; upstream_gene_variant; intron_variant | ||
Variant Effect | downstream_gene_variant(ENST00000403376, ENST00000360454, ENST00000481904, ENST00000467122); upstream_gene_variant(ENST00000428710); intron_variant(ENST00000373861) | ||
SIFT Annotation | tolerated_-_low_confidence; tolerated | ||
SIFT Variant Effect | tolerated_-_low_confidence(ENST00000360454); tolerated(ENST00000403376) | ||
PolyPhen Annotation | probably_damaging; possibly_damaging | ||
PolyPhen Variant Effect | probably_damaging(ENST00000403376); possibly_damaging(ENST00000360454) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | TF binding region;Chromatin interactive region | ||
Chromatin State | Enhancers;Weak transcription | ||
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.