Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs7123436
rs7123436
11 47991932 intron variant G/A snv 0.22
CUI: C0040420
Disease: Tonometry
Tonometry
0.700 1.000 2 2018 2018
dbSNP: rs4752805
rs4752805
11 47996803 intron variant A/C;G snv
CUI: C0040420
Disease: Tonometry
Tonometry
0.700 1.000 1 2018 2018