SNP Report
Name | rs141129523 dbSNP Ensembl | ||
---|---|---|---|
Location | 1:192814167 - 192814167(+) | ||
Variant Seq | G | ||
Ancestral Allele | A | ||
Ref Seq | A | ||
Minor Allele Frequence | 0.0119808 | ||
Annotation | downstream_gene_variant | ||
Variant Effect | downstream_gene_variant(ENST00000464302, ENST00000487236, ENST00000235382, ENST00000483295) | ||
SIFT Annotation | tolerated | ||
SIFT Variant Effect | tolerated(ENST00000235382) | ||
PolyPhen Annotation | possibly_damaging | ||
PolyPhen Variant Effect | possibly_damaging(ENST00000235382) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | Chromatin interactive region | ||
Chromatin State | Weak transcription;Enhancers;Flanking Active TSS | ||
No. of Marker's Association Results | 1 (Positive: 1; Negative: 0; Trend: 0) | ||
Source | Literature |