SNP Report
Name | rs213638 dbSNP Ensembl | ||
---|---|---|---|
Location | 1:25861747 - 25861747(+) | ||
Variant Seq | A | ||
Ancestral Allele | G | ||
Ref Seq | G | ||
Minor Allele Frequence | 0.488219 | ||
Annotation | upstream_gene_variant; 3_prime_UTR_variant; intron_variant; non_coding_transcript_variant | ||
Variant Effect | upstream_gene_variant(ENST00000374298, ENST00000538789); 3_prime_UTR_variant(ENST00000374296); intron_variant(ENST00000455431); non_coding_transcript_variant(ENST00000455431) | ||
SIFT Annotation | deleterious; tolerated | ||
SIFT Variant Effect | deleterious(ENST00000374296); tolerated(ENST00000374296) | ||
PolyPhen Annotation | benign | ||
PolyPhen Variant Effect | benign(ENST00000374296) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | TF binding region;Chromatin interactive region | ||
Chromatin State | Weak transcription;Enhancers;Flanking Active TSS;Genic enhancers;Strong transcription | ||
No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |