SNP Report
Name | rs11214599 dbSNP Ensembl | ||
---|---|---|---|
Location | 11:113400638 - 113400638(+) | ||
Variant Seq | T | ||
Ancestral Allele | C | ||
Ref Seq | C | ||
Minor Allele Frequence | 0.203275 | ||
Annotation | downstream_gene_variant; upstream_gene_variant | ||
Variant Effect | downstream_gene_variant(ENST00000303941, ENST00000542948); upstream_gene_variant(ENST00000546284) | ||
SIFT Annotation | tolerated | ||
SIFT Variant Effect | tolerated(ENST00000303941) | ||
PolyPhen Annotation | benign | ||
PolyPhen Variant Effect | benign(ENST00000303941) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | n/a | ||
Chromatin State | Weak transcription;Strong transcription | ||
No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |