SNP Report
Name | rs7933505 dbSNP Ensembl | ||
---|---|---|---|
Location | 11:18024440 - 18024440(+) | ||
Variant Seq | A | ||
Ancestral Allele | G | ||
Ref Seq | G | ||
Minor Allele Frequence | 0.289736 | ||
Annotation | upstream_gene_variant; intron_variant; NMD_transcript_variant | ||
Variant Effect | upstream_gene_variant(ENST00000525523, ENST00000525406); intron_variant(ENST00000417164, ENST00000250018); NMD_transcript_variant(ENST00000417164) | ||
SIFT Annotation | tolerated | ||
SIFT Variant Effect | tolerated(ENST00000250018) | ||
PolyPhen Annotation | possibly_damaging | ||
PolyPhen Variant Effect | possibly_damaging(ENST00000250018) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | TF binding region;Chromatin interactive region | ||
Chromatin State | Weak transcription | ||
No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |