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: rs1555625363
rs1555625363
2 0.925 0.080 16 89932649 missense variant C/T snv 0.700 1.000 1 2018 2018
dbSNP: rs1057518686
rs1057518686
1 1.000 16 89935433 missense variant G/A snv 0.700 0
dbSNP: rs1057521924
rs1057521924
1 1.000 16 89935313 missense variant G/A snv 0.700 0
dbSNP: rs267607165
rs267607165
18 0.708 0.520 16 89935679 missense variant G/A;C snv 0.700 0
dbSNP: rs587784505
rs587784505
3 0.882 0.160 16 89934743 missense variant G/A snv 0.700 0
dbSNP: rs878853279
rs878853279
1 1.000 16 89935613 missense variant A/G snv 0.700 0
dbSNP: rs878853256
rs878853256
1 1.000 16 89935418 missense variant A/G snv 0.800 1.000 1 2010 2010
dbSNP: rs878853257
rs878853257
1 1.000 16 89935064 missense variant G/A snv 0.800 1.000 1 2010 2010
dbSNP: rs878853258
rs878853258
1 1.000 16 89935356 missense variant C/T snv 0.800 1.000 1 2010 2010
dbSNP: rs747480526
rs747480526
1 1.000 16 89934984 missense variant C/T snv 4.0E-06 0.800 0