SNP Report
Name | rs13113036 dbSNP Ensembl | ||
---|---|---|---|
Location | 4:34133916 - 34133916(+) | ||
Variant Seq | C | ||
Ancestral Allele | A | ||
Ref Seq | A | ||
Minor Allele Frequence | 0.234026 | ||
Annotation | intron_variant; non_coding_transcript_variant | ||
Variant Effect | intron_variant(ENST00000514877, ENST00000513843); non_coding_transcript_variant(ENST00000514877, ENST00000513843) | ||
SIFT Annotation | deleterious; tolerated | ||
SIFT Variant Effect | deleterious(ENST00000621961); tolerated(ENST00000511884) | ||
PolyPhen Annotation | benign | ||
PolyPhen Variant Effect | benign(ENST00000511884, ENST00000621961) | ||
rSNP? | No Link in rVarBase | ||
Related Regulatory Elements | n/a | ||
Chromatin State | Inactive region | ||
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.