SNP Report
Name | rs3779247 dbSNP Ensembl | ||
---|---|---|---|
Location | 7:31061090 - 31061090(+) | ||
Variant Seq | G | ||
Ancestral Allele | G | ||
Ref Seq | C | ||
Minor Allele Frequence | 0.226837 | ||
Annotation | upstream_gene_variant; intron_variant | ||
Variant Effect | upstream_gene_variant(ENST00000409489, ENST00000396211); intron_variant(ENST00000409363, ENST00000614107, ENST00000304166, ENST00000431811) | ||
SIFT Annotation | deleterious | ||
SIFT Variant Effect | deleterious(ENST00000326139, ENST00000409904) | ||
PolyPhen Annotation | benign | ||
PolyPhen Variant Effect | benign(ENST00000326139, ENST00000409904) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | TF binding region | ||
Chromatin State | Enhancers;Weak transcription;Active TSS | ||
No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |