SNP Report
Name | rs2437772 dbSNP Ensembl | ||
---|---|---|---|
Location | 8:96500749 - 96500749(+) | ||
Variant Seq | T | ||
Ancestral Allele | T | ||
Ref Seq | C | ||
Minor Allele Frequence | 0.252596 | ||
Annotation | intron_variant; non_coding_transcript_variant | ||
Variant Effect | intron_variant(ENST00000522911, ENST00000518385, ENST00000302190, ENST00000519587, ENST00000520233); non_coding_transcript_variant(ENST00000519587, ENST00000520233) | ||
SIFT Annotation | deleterious; tolerated | ||
SIFT Variant Effect | deleterious(ENST00000518385); tolerated(ENST00000302190) | ||
PolyPhen Annotation | benign | ||
PolyPhen Variant Effect | benign(ENST00000518385, ENST00000302190) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | n/a | ||
Chromatin State | Weak transcription;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.