SNP Report
Name | rs11072768 dbSNP Ensembl | ||
---|---|---|---|
Location | 15:78637136 - 78637136(+) | ||
Variant Seq | G | ||
Ancestral Allele | T | ||
Ref Seq | T | ||
Minor Allele Frequence | 0.445687 | ||
Annotation | intron_variant; NMD_transcript_variant; non_coding_transcript_variant | ||
Variant Effect | intron_variant(ENST00000261751, ENST00000559849, ENST00000560511, ENST00000412074); NMD_transcript_variant(ENST00000559849); non_coding_transcript_variant(ENST00000560511) | ||
SIFT Annotation | tolerated_-_low_confidence; tolerated | ||
SIFT Variant Effect | tolerated_-_low_confidence(ENST00000412074); tolerated(ENST00000261751) | ||
PolyPhen Annotation | benign | ||
PolyPhen Variant Effect | benign(ENST00000261751, ENST00000412074) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | Chromatin interactive region | ||
Chromatin State | Weak transcription;Enhancers | ||
No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |