Home / Variant

chr1_3423901_A_G

chr1:3423901 · GRCh38AGrs1264931008receptor_confirmed

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

Receptor variant-effect scores

PXR
0.035Neutral
FXR
0.050Neutral
AhR
-0.088Neutral
-1 LoF0+1 GoF

Strongest effect: AhR Neutral at p99-scaled -0.088. 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
-0.28
dbSNP
rs1264931008
Region tier
receptor_confirmed

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

All substitutions at this position

SubstitutionPXRFXRAhRgnomAD AF
AC0.0040.0010.023not observed
AG0.0350.050-0.088not observed
AT-0.005-0.015-0.082not observed

Every possible base substitution at chr1:3423901, 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