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rare variant associated_with SNP

Subject
rare variant
Relation
associated_with
Object
SNP
p-value
Evidence from: primary | all sources

Evidence (2 sources)

Functionally informed fine-mapping and polygenic localization of complex trait heritability. (2020) PMID:33199916 cited
The 3,025 PIP>0.95 SNP‑trait pairs spanned 2,225 unique SNPs, including ... 185 rare SNPs (0.001<MAF<0.005).
confidence: 0.90
Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity. (2013) PMID:23563609 cited
Only directly genotyped SNPs for the discovery sample set were used ... to test for association with rare variants
confidence: 0.60