SNP Report
Name | rs2312236 dbSNP Ensembl | ||
---|---|---|---|
Location | 1:166824980 - 166824980(+) | ||
Variant Seq | C | ||
Ancestral Allele | C | ||
Ref Seq | T | ||
Minor Allele Frequence | 0.0654952 | ||
Annotation | downstream_gene_variant | ||
SIFT Annotation | deleterious | ||
SIFT Variant Effect | deleterious(ENST00000354422, ENST00000456900, ENST00000338353, ENST00000435676, ENST00000441649) | ||
PolyPhen Annotation | probably_damaging | ||
PolyPhen Variant Effect | probably_damaging(ENST00000354422, ENST00000456900, ENST00000338353, ENST00000435676, ENST00000441649) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | Chromatin interactive region | ||
Chromatin State | Inactive region | ||
No. of Marker's Association Results | 1 (Positive: 0; Negative: 0; Trend: 1) | ||
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.