rs457717, IQGAP2;F2RL2

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.
hearing impairment
CUI: C1384666
Disease: hearing impairment
337 5 76625147 intron variant A/G snv 0.65 0.810 1.000 2 2010 2016