SNP Report
Name | rs9538394 dbSNP Ensembl | ||
---|---|---|---|
Location | 13:59354287 - 59354287(+) | ||
Variant Seq | T | ||
Ancestral Allele | T | ||
Ref Seq | G | ||
Minor Allele Frequence | 0.457069 | ||
Annotation | downstream_gene_variant | ||
SIFT Annotation | deleterious_-_low_confidence | ||
SIFT Variant Effect | deleterious_-_low_confidence(ENST00000612954, ENST00000377918) | ||
PolyPhen Annotation | possibly_damaging; probably_damaging | ||
PolyPhen Variant Effect | possibly_damaging(ENST00000377918); probably_damaging(ENST00000612954) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | n/a | ||
Chromatin State | Weak transcription;Active TSS;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.