SNP Report
Name | rs11637635 dbSNP Ensembl | ||
---|---|---|---|
Location | 15:78584808 - 78584808(+) | ||
Variant Seq | G | ||
Ancestral Allele | A | ||
Ref Seq | A | ||
Minor Allele Frequence | 0.254593 | ||
Annotation | downstream_gene_variant; intron_variant | ||
Variant Effect | downstream_gene_variant(ENST00000567141); intron_variant(ENST00000299565, ENST00000559554, ENST00000394802) | ||
SIFT Annotation | tolerated_-_low_confidence; deleterious_-_low_confidence; tolerated | ||
SIFT Variant Effect | tolerated_-_low_confidence(ENST00000559554); deleterious_-_low_confidence(ENST00000394802); tolerated(ENST00000559576) | ||
PolyPhen Annotation | unknown; benign | ||
PolyPhen Variant Effect | unknown(ENST00000559554); benign(ENST00000394802, ENST00000559576) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | Chromatin interactive region | ||
Chromatin State | Weak transcription | ||
No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |