Disease Term Disease ID Gene Symbol Classification References Source
CHROMOSOME 16p11.2 DELETION SYNDROME, 220-KB C3150701 SH2B1 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
CHROMOSOME 16p11.2 DELETION SYNDROME, 593-KB C3150154 SH2B1 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -