SNP Report
Name | rs10226318 dbSNP Ensembl | ||
---|---|---|---|
Location | 7:31057843 - 31057843(+) | ||
Variant Seq | G | ||
Ancestral Allele | G | ||
Ref Seq | T | ||
Minor Allele Frequence | 0.366813 | ||
Annotation | intron_variant | ||
Variant Effect | intron_variant(ENST00000409363, ENST00000304166, ENST00000614107, ENST00000431811) | ||
SIFT Annotation | deleterious | ||
SIFT Variant Effect | deleterious(ENST00000326139, ENST00000409904) | ||
PolyPhen Annotation | benign | ||
PolyPhen Variant Effect | benign(ENST00000326139, ENST00000409904) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | Chromatin interactive region | ||
Chromatin State | Weak transcription;Active TSS;Enhancers;Bivalent Enhancer | ||
No. of Marker's Association Results | 1 (Positive: 0; Negative: 1; Trend: 0) | ||
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.