rare variant associated_with SNP
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