SNP Report
Name | rs276651 dbSNP Ensembl | ||
---|---|---|---|
Location | 8:72225852 - 72225852(+) | ||
Variant Seq | G | ||
Ancestral Allele | A | ||
Ref Seq | A | ||
Minor Allele Frequence | 0.150958 | ||
Annotation | intron_variant; non_coding_transcript_variant | ||
Variant Effect | intron_variant(ENST00000503430); non_coding_transcript_variant(ENST00000503430) | ||
SIFT Annotation | tolerated | ||
SIFT Variant Effect | tolerated(ENST00000262209) | ||
PolyPhen Annotation | benign | ||
PolyPhen Variant Effect | benign(ENST00000262209) | ||
rSNP? | No Link in rVarBase | ||
Related Regulatory Elements | n/a | ||
Chromatin State | Inactive region | ||
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.