credible_set
Identifier
Section titled “Identifier”Description
Section titled “Description”95% credible sets for GWAS and molQTL studies.
Credible sets include all variants in the credible set as well as the fine-mapping method and statistics used to estimate the credible set [Genetics]
Partitions
Section titled “Partitions”release'26.06'
Schema
Section titled “Schema”| Column | Type | Description |
|---|---|---|
studyLocusId |
TEXT |
Study-locus identifier for the credible set |
studyId |
TEXT |
Identifier for the study which the credible set is derived |
variantId |
TEXT |
The lead variant for the credible set, by posterior probability |
chromosome |
TEXT |
Chromosome which the credible set is located |
position |
INT |
Position of the lead variant for the credible set (GRCh38) |
region |
TEXT |
Start and end positions of the region used for fine-mapping |
beta |
DOUBLE |
Beta coefficient of the lead variant |
zScore |
DOUBLE |
Z-score of the lead variant from the GWAS |
pValueMantissa |
FLOAT |
Mantissa value of the lead variant P-value |
pValueExponent |
INT |
Exponent value of the lead variant P-value |
effectAlleleFrequencyFromSource |
FLOAT |
Allele frequency of the lead variant from the GWAS |
standardError |
DOUBLE |
Standard error of the lead variant |
subStudyDescription |
TEXT |
[Deprecated] |
qualityControls |
TEXT[] |
Quality control flags for this credible set |
finemappingMethod |
TEXT |
Method used for fine-mapping of credible set |
credibleSetIndex |
INT |
Integer label for the order of credible sets from study-region |
credibleSetlog10BF |
DOUBLE |
Log10 Bayes factor for the entire credible set |
purityMeanR2 |
DOUBLE |
Mean R-squared linkage disequilibrium for variants in the credible set |
purityMinR2 |
DOUBLE |
Minimum R-squared linkage disequilibrium for variants in the credible set |
locusStart |
INT |
Start position of the region that was fine-mapped for this credible set |
locusEnd |
INT |
End position of the region that was fine-mapped for this credible set |
sampleSize |
INT |
Sample size of the study from which this credible set is derived |
ldSet |
STRUCT(tagVariantId TEXT, r2Overall DOUBLE)[] |
Array of structs which denote the variants in LD with the credible set lead variant |
locus |
STRUCT(is95CredibleSet BOOLEAN, is99CredibleSet BOOLEAN, logBF DOUBLE, posteriorProbability DOUBLE, variantId TEXT, pValueMantissa FLOAT, pValueExponent INT, beta DOUBLE, standardError DOUBLE, r2Overall DOUBLE)[] |
Array of structs which denote the variants within the credible set |
confidence |
TEXT |
Description of how this credible set was derived in terms of data and fine-mapping method |
studyType |
TEXT |
Descriptor for whether the credible set is derived from GWAS or molecular QTL |
isTransQtl |
BOOLEAN |
Boolean for whether this credible set is a trans-pQTL or not |
release |
TEXT |
Partition column. Open Targets Platform release version (major.minor), e.g. 26.06. [Added during ingest.] |