SNP Report
Name | rs142570922 dbSNP Ensembl | ||
---|---|---|---|
Location | 8:142881701 - 142881701(+) | ||
Variant Seq | C | ||
Ref Seq | A | ||
Annotation | upstream_gene_variant; intron_variant | ||
Variant Effect | upstream_gene_variant(ENST00000377675, ENST00000292427, ENST00000314111, ENST00000517471); intron_variant(ENST00000522728) | ||
SIFT Annotation | tolerated | ||
SIFT Variant Effect | tolerated(ENST00000292427, ENST00000377675, ENST00000517471) | ||
PolyPhen Annotation | benign | ||
PolyPhen Variant Effect | benign(ENST00000292427, ENST00000377675, ENST00000517471) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | n/a | ||
Chromatin State | Weak transcription | ||
No. of Marker's Association Results | 1 (Positive: 0; Negative: 0; Trend: 1) | ||
Source | Literature |