Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1343795
rs1343795
ZNF652
5 0.882 0.120 17 49334880 intron variant C/A snv 0.78 0.010 1.000 1 2018 2018
dbSNP: rs4572450
rs4572450
ZNF652
4 0.882 0.120 17 49343367 intron variant T/C snv 0.78 0.010 1.000 1 2018 2018
dbSNP: rs976078
rs976078 		4 0.882 0.120 13 82963398 intron variant A/C snv 0.15 0.010 1.000 1 2018 2018