rs760929207, OBSL1

N. diseases: 12
Disease: Long narrow head ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Long narrow head
CUI: C0221358
Disease: Long narrow head
0.700 GeneticVariation CLINVAR Further expanding the mutational spectrum and investigation of genotype-phenotype correlation in 3M syndrome. 30980518 2019