SNP Report
Name | rs10741734 dbSNP Ensembl | ||
---|---|---|---|
Location | 11:18023101 - 18023101(+) | ||
Variant Seq | G | ||
Ancestral Allele | G | ||
Ref Seq | A | ||
Minor Allele Frequence | 0.324281 | ||
Annotation | non_coding_transcript_exon_variant; upstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_variant | ||
Variant Effect | non_coding_transcript_exon_variant(ENST00000525406); upstream_gene_variant(ENST00000525523); intron_variant(ENST00000250018, ENST00000417164); NMD_transcript_variant(ENST00000417164); non_coding_transcript_variant(ENST00000525406) | ||
SIFT Annotation | tolerated | ||
SIFT Variant Effect | tolerated(ENST00000250018) | ||
PolyPhen Annotation | benign | ||
PolyPhen Variant Effect | benign(ENST00000250018) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | Chromatin interactive region | ||
Chromatin State | Weak transcription | ||
No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |