SNP Report
Name | rs11909487 dbSNP Ensembl | ||
---|---|---|---|
Location | 21:15690060 - 15690060(+) | ||
Variant Seq | C | ||
Ancestral Allele | C | ||
Ref Seq | T | ||
Minor Allele Frequence | 0.41853 | ||
Annotation | downstream_gene_variant; upstream_gene_variant | ||
Variant Effect | downstream_gene_variant(ENST00000454157); upstream_gene_variant(ENST00000408570) | ||
SIFT Annotation | tolerated | ||
SIFT Variant Effect | tolerated(ENST00000400202, ENST00000318948, ENST00000400199) | ||
PolyPhen Annotation | benign | ||
PolyPhen Variant Effect | benign(ENST00000400202, ENST00000318948, ENST00000400199) | ||
rSNP? | No Link in rVarBase | ||
Related Regulatory Elements | N.A. | ||
Chromatin State | N.A. | ||
No. of Marker's Association Results | 1 (Positive: 0; Negative: 0; Trend: 1) | ||
Source | Literature |