SNP Report
Name | rs9868039 dbSNP Ensembl | ||
---|---|---|---|
Location | 3:114127695 - 114127695(+) | ||
Variant Seq | A | ||
Ancestral Allele | A | ||
Ref Seq | G | ||
Minor Allele Frequence | 0.457867 | ||
Annotation | downstream_gene_variant | ||
Variant Effect | downstream_gene_variant(ENST00000460779, ENST00000467632, ENST00000295881, ENST00000383673) | ||
SIFT Annotation | deleterious | ||
SIFT Variant Effect | deleterious(ENST00000460779, ENST00000467632, ENST00000295881, ENST00000383673) | ||
PolyPhen Annotation | possibly_damaging; probably_damaging | ||
PolyPhen Variant Effect | possibly_damaging(ENST00000295881); probably_damaging(ENST00000460779, ENST00000467632, ENST00000383673) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | n/a | ||
Chromatin State | Weak transcription | ||
No. of Marker's Association Results | 1 (Positive: 1; Negative: 0; Trend: 0) | ||
Source | Literature |