SNP Report
Name | rs8078495 dbSNP Ensembl | ||
---|---|---|---|
Location | 17:45923244 - 45923244(+) | ||
Variant Seq | A,T | ||
Ancestral Allele | G | ||
Ref Seq | G | ||
Minor Allele Frequence | 0.0860623 | ||
Annotation | intron_variant; NMD_transcript_variant; non_coding_transcript_variant | ||
Variant Effect | intron_variant(ENST00000535772, ENST00000334239, ENST00000351559, ENST00000570299, ENST00000340799, ENST00000344290, ENST00000571311, ENST00000262410, ENST00000446361); NMD_transcript_variant(ENST00000571311); non_coding_transcript_variant(ENST00000570299) | ||
SIFT Annotation | tolerated | ||
SIFT Variant Effect | tolerated(ENST00000329196) | ||
PolyPhen Annotation | benign | ||
PolyPhen Variant Effect | benign(ENST00000329196) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | Chromatin interactive region | ||
Chromatin State | Enhancers;Genic enhancers;Weak transcription | ||
No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |