SNP Report
Name | rs1415265 dbSNP Ensembl | ||
---|---|---|---|
Location | 1:162137172 - 162137172(+) | ||
Variant Seq | T | ||
Ancestral Allele | C | ||
Ref Seq | C | ||
Minor Allele Frequence | 0.423922 | ||
Annotation | intron_variant; NMD_transcript_variant | ||
Variant Effect | intron_variant(ENST00000361897, ENST00000430120, ENST00000530878); NMD_transcript_variant(ENST00000430120) | ||
SIFT Annotation | tolerated | ||
SIFT Variant Effect | tolerated(ENST00000361897, ENST00000530878, ENST00000430120) | ||
PolyPhen Annotation | benign | ||
PolyPhen Variant Effect | benign(ENST00000361897, ENST00000530878, ENST00000430120) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | Chromatin interactive region | ||
Chromatin State | Enhancers;Weak transcription;Flanking Active TSS | ||
No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |