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chr9_6681505_C_G

chr9:6681505 · GRCh38CGrs116937669gnomAD AF 1.98%receptor_confirmed

Regulatory target ENSG00000225489 is taken from a GTEx liver eQTL, not from distance. For a non-coding regulatory variant the nearest gene by distance is frequently not the regulated gene.

Receptor variant-effect scores

PXR
-0.487LoF
FXR
-0.182LoF
AhR
-0.235LoF
-1 LoF0+1 GoF

Strongest effect: PXR LoF at p99-scaled -0.487. 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

GTEx liver eQTL
ENSG00000225489, slope 0.85, p 5.7e-7
phyloP conservation
-1.47
gnomAD
AF 1.98%
dbSNP
rs116937669
Region tier
receptor_confirmed

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

All substitutions at this position

SubstitutionPXRFXRAhRgnomAD AF
CA-0.330-0.204-0.261not observed
CG-0.487-0.182-0.2351.98%
CT-0.511-0.214-0.2090.040%

Every possible base substitution at chr9:6681505, 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: AhR