SNP Report
Name | rs1607395 dbSNP Ensembl | ||
---|---|---|---|
Location | 11:18028189 - 18028189(+) | ||
Variant Seq | C | ||
Ancestral Allele | C | ||
Ref Seq | T | ||
Minor Allele Frequence | 0.324081 | ||
Annotation | downstream_gene_variant; intron_variant; NMD_transcript_variant | ||
Variant Effect | downstream_gene_variant(ENST00000528338); intron_variant(ENST00000417164, ENST00000250018); NMD_transcript_variant(ENST00000417164) | ||
SIFT Annotation | deleterious; tolerated | ||
SIFT Variant Effect | deleterious(ENST00000528338); tolerated(ENST00000250018, ENST00000417164) | ||
PolyPhen Annotation | benign; possibly_damaging | ||
PolyPhen Variant Effect | benign(ENST00000250018, ENST00000417164); possibly_damaging(ENST00000528338) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | n/a | ||
Chromatin State | Weak transcription;Enhancers | ||
No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |