SNP Report
Name | rs2616978 dbSNP Ensembl | ||
---|---|---|---|
Location | 8:4620822 - 4620822(+) | ||
Variant Seq | C | ||
Ancestral Allele | T | ||
Ref Seq | T | ||
Minor Allele Frequence | 0.492412 | ||
Annotation | intron_variant | ||
Variant Effect | intron_variant(ENST00000602557, ENST00000602723, ENST00000400186, ENST00000635120, ENST00000520002) | ||
SIFT Annotation | tolerated | ||
SIFT Variant Effect | tolerated(ENST00000520002, ENST00000602723, ENST00000635120, ENST00000602557, ENST00000400186) | ||
PolyPhen Annotation | benign | ||
PolyPhen Variant Effect | benign(ENST00000520002, ENST00000602723, ENST00000635120, ENST00000602557, ENST00000400186) | ||
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.