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: rs397514699
rs397514699
1 1.000 19 919949 missense variant C/A;T snv 3.5E-05; 5.8E-06 0.800 1.000 6 2003 2014
dbSNP: rs104894703
rs104894703
3 0.882 0.040 19 918604 missense variant T/C snv 2.5E-05 1.4E-05 0.700 1.000 6 2003 2014
dbSNP: rs144670595
rs144670595
2 0.925 0.120 19 920441 missense variant G/T snv 3.3E-04 4.5E-04 0.700 1.000 6 2003 2014
dbSNP: rs28939719
rs28939719
3 0.882 0.040 19 919563 missense variant T/C snv 0.700 1.000 6 2003 2014
dbSNP: rs73507527
rs73507527
1 1.000 19 919933 missense variant G/A;T snv 4.6E-03; 6.0E-06 0.700 1.000 6 2003 2014
dbSNP: rs745580229
rs745580229
1 1.000 19 920336 missense variant C/T snv 6.0E-06 0.700 1.000 6 2003 2014