SNP Report
Name | rs75431302 dbSNP Ensembl | ||
---|---|---|---|
Location | 8:42707876 - 42707876(+) | ||
Variant Seq | C | ||
Ancestral Allele | G | ||
Ref Seq | G | ||
Minor Allele Frequence | 0.00698882 | ||
Annotation | intron_variant; non_coding_transcript_variant | ||
Variant Effect | intron_variant(ENST00000289957, ENST00000527318, ENST00000534391, ENST00000531610); non_coding_transcript_variant(ENST00000527318, ENST00000531610) | ||
SIFT Annotation | tolerated | ||
SIFT Variant Effect | tolerated(ENST00000289957) | ||
PolyPhen Annotation | possibly_damaging | ||
PolyPhen Variant Effect | possibly_damaging(ENST00000289957) | ||
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 |