SNP Report
Name | rs10241138 dbSNP Ensembl | ||
---|---|---|---|
Location | 7:31056747 - 31056747(+) | ||
Variant Seq | C | ||
Ancestral Allele | T | ||
Ref Seq | T | ||
Minor Allele Frequence | 0.185903 | ||
Annotation | upstream_gene_variant; intron_variant | ||
Variant Effect | upstream_gene_variant(ENST00000431811); intron_variant(ENST00000409363, ENST00000304166, ENST00000614107) | ||
SIFT Annotation | deleterious | ||
SIFT Variant Effect | deleterious(ENST00000326139, ENST00000409904) | ||
PolyPhen Annotation | benign | ||
PolyPhen Variant Effect | benign(ENST00000326139, ENST00000409904) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | TF binding region;Chromatin interactive region | ||
Chromatin State | Enhancers;Weak transcription;Active TSS;Bivalent Enhancer | ||
No. of Marker's Association Results | 1 (Positive: 0; Negative: 1; Trend: 0) | ||
Source | Literature |