Home / Variant

chr1_16498941_T_G

chr1:16498941 · GRCh38TGrs1205814218receptor_confirmed

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

Receptor variant-effect scores

PXR
-0.046Neutral
FXR
-0.070Neutral
AhR
-0.602LoF
-1 LoF0+1 GoF

Strongest effect: AhR LoF at p99-scaled -0.602. Impact is large relative to 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
-2.85
dbSNP
rs1205814218
Region tier
receptor_confirmed

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

All substitutions at this position

SubstitutionPXRFXRAhRgnomAD AF
TA0.017-0.019-0.111not observed
TC-0.053-0.055-0.421not observed
TG-0.046-0.070-0.602not observed

Every possible base substitution at chr1:16498941, 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