SNP Report
Name | rs74572794 dbSNP Ensembl | ||
---|---|---|---|
Location | 8:42774242 - 42774242(+) | ||
Variant Seq | A | ||
Ancestral Allele | C | ||
Ref Seq | C | ||
Minor Allele Frequence | 0.0595048 | ||
Annotation | intron_variant | ||
Variant Effect | intron_variant(ENST00000533810) | ||
SIFT Annotation | deleterious | ||
SIFT Variant Effect | deleterious(ENST00000534622, ENST00000276410) | ||
PolyPhen Annotation | probably_damaging | ||
PolyPhen Variant Effect | probably_damaging(ENST00000534622, ENST00000276410) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | n/a | ||
Chromatin State | Weak transcription;Enhancers | ||
No. of Marker's Association Results | 1 (Positive: 0; Negative: 1; Trend: 0) | ||
Source | Literature |