SNP Report
Name | rs17104851 dbSNP Ensembl | ||
---|---|---|---|
Location | 12:68137564 - 68137564(+) | ||
Variant Seq | A | ||
Ancestral Allele | C | ||
Ref Seq | C | ||
Minor Allele Frequence | 0.167732 | ||
Annotation | intron_variant; non_coding_transcript_variant | ||
Variant Effect | intron_variant(ENST00000536914); non_coding_transcript_variant(ENST00000536914) | ||
SIFT Annotation | tolerated | ||
SIFT Variant Effect | tolerated(ENST00000393555, ENST00000344096) | ||
PolyPhen Annotation | benign | ||
PolyPhen Variant Effect | benign(ENST00000393555, ENST00000344096) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | n/a | ||
Chromatin State | Bivalent Enhancer;Flanking Active TSS;Enhancers | ||
No. of Marker's Association Results | 1 (Positive: 0; Negative: 0; Trend: 1) | ||
Source | Literature |
The LD data used here is based on 1000 Genome Phase I. LD SNP pairs were selected with a threshold r2<=0.8.