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chr2_9951672_C_T

chr2:9951672 · GRCh38CTrs1666766645receptor_confirmed

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

Receptor variant-effect scores

PXR
-0.003Neutral
FXR
0.051Neutral
AhR
0.264GoF
-1 LoF0+1 GoF

Strongest effect: AhR GoF at p99-scaled 0.264. 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

phyloP conservation
0.92
dbSNP
rs1666766645
Region tier
receptor_confirmed

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

All substitutions at this position

SubstitutionPXRFXRAhRgnomAD AF
CA0.0050.0410.219not observed
CG0.0620.0180.123not observed
CT-0.0030.0510.264not observed

Every possible base substitution at chr2:9951672, 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