SNP Report
Name | rs129915 dbSNP Ensembl | ||
---|---|---|---|
Location | 9:133659796 - 133659796(+) | ||
Variant Seq | G | ||
Ancestral Allele | G | ||
Ref Seq | A | ||
Minor Allele Frequence | 0.269768 | ||
Annotation | downstream_gene_variant; upstream_gene_variant | ||
Variant Effect | downstream_gene_variant(ENST00000371868, ENST00000371872, ENST00000422262, ENST00000393056, ENST00000439388, ENST00000469828); upstream_gene_variant(ENST00000425189) | ||
SIFT Annotation | tolerated_-_low_confidence | ||
SIFT Variant Effect | tolerated_-_low_confidence(ENST00000371868) | ||
PolyPhen Annotation | benign | ||
PolyPhen Variant Effect | benign(ENST00000371868) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | TF binding region;Chromatin interactive region;lncRNA | ||
Chromatin State | Bivalent Enhancer;Enhancers;Weak transcription | ||
No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |