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: rs376239580
rs376239580
2 0.925 0.040 20 5302632 missense variant G/A snv 1.2E-05 2.1E-05 0.700 0
dbSNP: rs146544539
rs146544539
1 1.000 0.040 20 5302386 missense variant C/T snv 1.0E-04 2.8E-05 0.010 1.000 1 2019 2019
dbSNP: rs774883653
rs774883653
1 1.000 0.040 20 5302542 missense variant A/G snv 4.8E-05 4.2E-05 0.010 1.000 1 2019 2019