SNP Report
Name | rs77929608 dbSNP Ensembl | ||
---|---|---|---|
Location | 2:31584023 - 31584023(+) | ||
Variant Seq | G | ||
Ancestral Allele | G | ||
Ref Seq | C | ||
Minor Allele Frequence | 0.0607029 | ||
Annotation | upstream_gene_variant | ||
Variant Effect | upstream_gene_variant(ENST00000622030) | ||
SIFT Annotation | deleterious | ||
SIFT Variant Effect | deleterious(ENST00000622030) | ||
PolyPhen Annotation | benign | ||
PolyPhen Variant Effect | benign(ENST00000622030) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | TF binding region | ||
Chromatin State | Enhancers;Bivalent Enhancer;Weak transcription | ||
No. of Marker's Association Results | 1 (Positive: 1; Negative: 0; Trend: 0) | ||
Source | Literature |