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: rs267607162
rs267607162
1 1.000 0.160 16 89935235 missense variant C/T snv 0.800 1.000 1 2010 2010
dbSNP: rs267607163
rs267607163
1 1.000 0.160 16 89935355 missense variant G/A snv 0.800 1.000 1 2010 2010
dbSNP: rs267607164
rs267607164
2 0.925 0.160 16 89935700 missense variant G/A;C snv 0.800 1.000 1 2010 2010
dbSNP: rs267607165
rs267607165
18 0.708 0.520 16 89935679 missense variant G/A;C snv 0.800 1.000 1 2010 2010
dbSNP: rs864321717
rs864321717
1 1.000 0.160 16 89935589 missense variant C/T snv 0.800 1.000 1 2010 2010
dbSNP: rs587784505
rs587784505
3 0.882 0.160 16 89934743 missense variant G/A snv 0.700 0
dbSNP: rs864321714
rs864321714
1 1.000 0.160 16 89933486 missense variant G/A snv 0.700 0
dbSNP: rs864321715
rs864321715
1 1.000 0.160 16 89933512 missense variant G/A snv 0.700 0
dbSNP: rs864321716
rs864321716
1 1.000 0.160 16 89935236 missense variant G/A snv 0.700 0