PLCXD2 + 229 (Benign neoplasm of unspecified sites)

Go to gene PLCXD2 Go to pheno 229

pval: 0.017

Number of Rare Variants: 51

Chrom : Start - End: 3 : 111,675,304 - 111,845,857

Minor Allele Count in Cases / Controls: 7.0 / 251.0

Number of Cases / Controls: 284 / 28116