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: rs34595252
rs34595252
2 0.925 0.040 5 111119021 missense variant A/G snv 4.3E-03 4.5E-03 0.020 1.000 2 2005 2006
dbSNP: rs10038177
rs10038177
3 0.925 0.040 5 111100751 intron variant C/T snv 0.53 0.54 0.010 1.000 1 2017 2017
dbSNP: rs116529882
rs116529882
2 0.925 0.040 5 111110280 missense variant G/A snv 7.5E-04 8.9E-04 0.010 1.000 1 2005 2005
dbSNP: rs13178997
rs13178997
2 0.925 0.040 5 111108550 intron variant G/A;T snv 0.010 1.000 1 2017 2017
dbSNP: rs1438561194
rs1438561194
1 1.000 0.040 5 111092304 missense variant G/A snv 4.0E-06 7.0E-06 0.010 1.000 1 2012 2012
dbSNP: rs35703638
rs35703638
1 1.000 0.040 5 111106140 missense variant G/A snv 8.3E-03 4.1E-03 0.010 1.000 1 2005 2005