rs10180371, PARD3B

N. diseases: 1
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Tonometry
CUI: C0040420
Disease: Tonometry
573 2 205150255 intron variant A/G snv 0.64 0.700 1.000 1 2018 2018