Home / Variant

chr19_44616009_G_T

chr19:44616009 · GRCh38GTrs1039169153receptor_confirmed

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

Receptor variant-effect scores

PXR
0.394GoF
FXR
0.495GoF
AhR
0.447GoF
-1 LoF0+1 GoF

Strongest effect: FXR GoF at p99-scaled 0.495. 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
-0.53
dbSNP
rs1039169153
Region tier
receptor_confirmed

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

All substitutions at this position

SubstitutionPXRFXRAhRgnomAD AF
GA0.1820.1550.191not observed
GC0.6520.7920.694not observed
GT0.3940.4950.447not observed

Every possible base substitution at chr19:44616009, 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: FXR