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chr22_36028402_A_C

chr22:36028402 · GRCh38ACrs764216096gnomAD AF 100.0%receptor_confirmed

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

Receptor variant-effect scores

PXR
-0.039Neutral
FXR
-0.021Neutral
AhR
-0.262LoF
-1 LoF0+1 GoF

Strongest effect: AhR LoF at p99-scaled -0.262. Impact is moderate 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

ClinVar
Benign
phyloP conservation
-0.00
gnomAD
AF 100.0%
dbSNP
rs764216096
Region tier
receptor_confirmed

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

All substitutions at this position

SubstitutionPXRFXRAhRgnomAD AF
AC-0.039-0.021-0.262100.0%
AG-0.029-0.008-0.124not observed
AT-0.019-0.009-0.085not observed

Every possible base substitution at chr22:36028402, 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