SNP Report
Name | rs1076153 dbSNP Ensembl | ||
---|---|---|---|
Location | 9:133633021 - 133633021(+) | ||
Variant Seq | T | ||
Ancestral Allele | G | ||
Ref Seq | G | ||
Minor Allele Frequence | 0.352835 | ||
Annotation | non_coding_transcript_exon_variant; upstream_gene_variant; non_coding_transcript_variant | ||
Variant Effect | non_coding_transcript_exon_variant(ENST00000564021); upstream_gene_variant(ENST00000263611, ENST00000393056); non_coding_transcript_variant(ENST00000564021) | ||
SIFT Annotation | deleterious | ||
SIFT Variant Effect | deleterious(ENST00000356873, ENST00000496132) | ||
PolyPhen Annotation | possibly_damaging | ||
PolyPhen Variant Effect | possibly_damaging(ENST00000356873, ENST00000496132) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | TF binding region;lncRNA | ||
Chromatin State | Enhancers;Weak transcription;Bivalent Enhancer | ||
No. of Marker's Association Results | 1 (Positive: 0; Negative: 1; Trend: 0) | ||
Source | Literature |
The LD data used here is based on 1000 Genome Phase I. LD SNP pairs were selected with a threshold r2<=0.8.