SNP Report
Name | rs692780 dbSNP Ensembl | ||
---|---|---|---|
Location | 15:78584163 - 78584163(+) | ||
Variant Seq | G | ||
Ancestral Allele | G | ||
Ref Seq | C | ||
Minor Allele Frequence | 0.240016 | ||
Annotation | downstream_gene_variant; intron_variant | ||
Variant Effect | downstream_gene_variant(ENST00000567141); intron_variant(ENST00000559554, ENST00000299565, ENST00000394802) | ||
SIFT Annotation | deleterious | ||
SIFT Variant Effect | deleterious(ENST00000559576, ENST00000299565) | ||
PolyPhen Annotation | probably_damaging | ||
PolyPhen Variant Effect | probably_damaging(ENST00000559576, ENST00000299565) | ||
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 |