SNP Report
Name | rs11168070 dbSNP Ensembl | ||
---|---|---|---|
Location | 5:148826364 - 148826364(+) | ||
Variant Seq | C | ||
Ancestral Allele | C | ||
Ref Seq | G | ||
Minor Allele Frequence | 0.204073 | ||
Annotation | 5_prime_UTR_variant | ||
Variant Effect | 5_prime_UTR_variant(ENST00000305988) | ||
SIFT Annotation | deleterious | ||
SIFT Variant Effect | deleterious(ENST00000305988) | ||
PolyPhen Annotation | probably_damaging | ||
PolyPhen Variant Effect | probably_damaging(ENST00000305988) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | TF binding region;CpG island;Chromatin interactive region | ||
Chromatin State | Active TSS;Bivalent/Poised TSS;Flanking Bivalent TSS/Enh;Flanking Active TSS;Transcr. at gene 5' nd 3' | ||
No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |