SNP Report
Name | rs7784067 dbSNP Ensembl | ||
---|---|---|---|
Location | 7:31044484 - 31044484(+) | ||
Variant Seq | C | ||
Ancestral Allele | C | ||
Ref Seq | T | ||
Minor Allele Frequence | 0.478435 | ||
Annotation | upstream_gene_variant; intron_variant | ||
SIFT Annotation | deleterious | ||
SIFT Variant Effect | deleterious(ENST00000326139, ENST00000409904) | ||
PolyPhen Annotation | benign | ||
PolyPhen Variant Effect | benign(ENST00000326139, ENST00000409904) | ||
rSNP? | No Link in rVarBase | ||
Related Regulatory Elements | n/a | ||
Chromatin State | Inactive region | ||
No. of Marker's Association Results | 1 (Positive: 0; Negative: 1; Trend: 0) | ||
Source | Literature |