SNP Report
Name | rs7756263 dbSNP Ensembl | ||
---|---|---|---|
Location | 6:149032140 - 149032140(+) | ||
Variant Seq | T | ||
Ancestral Allele | A | ||
Ref Seq | A | ||
Minor Allele Frequence | 0.221246 | ||
Annotation | intron_variant; non_coding_transcript_variant | ||
Variant Effect | intron_variant(ENST00000433442, ENST00000367463); non_coding_transcript_variant(ENST00000433442) | ||
SIFT Annotation | deleterious | ||
SIFT Variant Effect | deleterious(ENST00000367463) | ||
PolyPhen Annotation | benign | ||
PolyPhen Variant Effect | benign(ENST00000367463) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | Chromatin interactive region | ||
Chromatin State | Weak transcription;Enhancers;Genic enhancers;Flanking Active TSS;Active TSS;Strong transcription | ||
No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |