SNP Report
Name | rs680244 dbSNP Ensembl | ||
---|---|---|---|
Location | 15:78578946 - 78578946(+) | ||
Variant Seq | C | ||
Ancestral Allele | C | ||
Ref Seq | T | ||
Minor Allele Frequence | 0.329073 | ||
Annotation | upstream_gene_variant; intron_variant | ||
Variant Effect | upstream_gene_variant(ENST00000394802); intron_variant(ENST00000559554, ENST00000299565) | ||
SIFT Annotation | deleterious | ||
SIFT Variant Effect | deleterious(ENST00000299565) | ||
PolyPhen Annotation | probably_damaging | ||
PolyPhen Variant Effect | probably_damaging(ENST00000299565) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | n/a | ||
Chromatin State | Weak transcription | ||
No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |