Home / Variant

chr1_147080683_G_T

chr1:147080683 · GRCh38GTrs1650586933receptor_confirmed

For a non-coding regulatory variant the nearest gene by distance is frequently not the regulated gene.

Receptor variant-effect scores

PXR
-0.023Neutral
FXR
0.018Neutral
AhR
-0.123LoF
-1 LoF0+1 GoF

Strongest effect: AhR LoF at p99-scaled -0.123. Impact is small on the receptor-specific p99 scale.

The p99-scaled score divides the raw delta by the receptor-specific 99th percentile of |delta| in the reference peak population, then clips to −1 to 1. It is a comparable effect scale, not a percentile rank. AhR is exploratory, from a single replicate.

Cross-annotations

phyloP conservation
-0.30
dbSNP
rs1650586933
Region tier
receptor_confirmed

Mirrored from ClinVar, GTEx, GWAS Catalog, JASPAR/FIMO, gnomAD and phyloP. See Databases.

All substitutions at this position

SubstitutionPXRFXRAhRgnomAD AF
GA-0.0100.016-0.047not observed
GC-0.0200.014-0.076not observed
GT-0.0230.018-0.123not observed

Every possible base substitution at chr1:147080683, each scored independently and shown as p99-scaled scores. The gnomAD column shows which substitution is actually seen in the population versus in silico only. Region confidence is the same for every substitution at this position, so it is shown once in the section below.

Region confidence

In receptor peaks: PXR