SNP Report
Name | rs564585 dbSNP Ensembl | ||
---|---|---|---|
Location | 15:78593885 - 78593885(+) | ||
Variant Seq | G | ||
Ancestral Allele | A | ||
Ref Seq | A | ||
Minor Allele Frequence | 0.444489 | ||
Annotation | downstream_gene_variant; upstream_gene_variant; 3_prime_UTR_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_variant | ||
Variant Effect | downstream_gene_variant(ENST00000559576, ENST00000326828, ENST00000394802, ENST00000559554); upstream_gene_variant(ENST00000567141); 3_prime_UTR_variant(ENST00000299565); intron_variant(ENST00000348639, ENST00000559002, ENST00000559658); NMD_transcript_variant(ENST00000559658); non_coding_transcript_variant(ENST00000559002) | ||
SIFT Annotation | tolerated | ||
SIFT Variant Effect | tolerated(ENST00000326828, ENST00000559658, ENST00000348639) | ||
PolyPhen Annotation | benign | ||
PolyPhen Variant Effect | benign(ENST00000326828, ENST00000559658, ENST00000348639) | ||
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 |