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: rs180177038
rs180177038
4 0.851 0.200 7 140778007 missense variant C/G;T snv 0.700 1.000 3 2006 2009
dbSNP: rs1554333853
rs1554333853
54 0.689 0.320 7 40046006 missense variant A/G snv 0.700 1.000 1 2017 2017
dbSNP: rs1232880706
rs1232880706
36 0.689 0.440 15 48526247 stop gained C/A;T snv 0.700 0
dbSNP: rs66527965
rs66527965
31 0.763 0.240 17 50193038 missense variant C/A;T snv 0.700 0
dbSNP: rs760805
rs760805
9 0.776 0.240 1 24925432 intron variant A/T snv 0.42 0.010 1.000 1 2019 2019