SNP Report
Name | rs9545302 dbSNP Ensembl | ||
---|---|---|---|
Location | 13:80027976 - 80027976(+) | ||
Variant Seq | C | ||
Ancestral Allele | A | ||
Ref Seq | A | ||
Minor Allele Frequence | 0.476637 | ||
Annotation | non_coding_transcript_exon_variant; non_coding_transcript_variant | ||
Variant Effect | non_coding_transcript_exon_variant(ENST00000627044); non_coding_transcript_variant(ENST00000627044) | ||
SIFT Annotation | tolerated | ||
SIFT Variant Effect | tolerated(ENST00000487865, ENST00000612570, ENST00000620924, ENST00000218652) | ||
PolyPhen Annotation | possibly_damaging; probably_damaging | ||
PolyPhen Variant Effect | possibly_damaging(ENST00000612570, ENST00000620924, ENST00000218652); probably_damaging(ENST00000487865) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | n/a | ||
Chromatin State | Weak transcription | ||
No. of Marker's Association Results | 1 (Positive: 0; Negative: 0; Trend: 1) | ||
Source | Literature |