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: rs11671664
rs11671664
5 0.925 0.120 19 45669020 intron variant G/A snv 0.12 0.700 1.000 4 2012 2017
dbSNP: rs11672660
rs11672660
5 19 45676926 intron variant C/T snv 0.18 0.17 0.700 1.000 3 2015 2019
dbSNP: rs1800437
rs1800437
13 0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17 0.700 1.000 3 2017 2019
dbSNP: rs10423928
rs10423928
12 0.807 0.200 19 45679046 intron variant T/A snv 0.19 0.700 1.000 1 2019 2019
dbSNP: rs139215588
rs139215588
1 19 45674762 missense variant G/A snv 4.9E-04 4.6E-04 0.700 1.000 1 2018 2018
dbSNP: rs143430880
rs143430880
1 19 45677718 missense variant A/G snv 1.4E-03 1.1E-03 0.700 1.000 1 2018 2018
dbSNP: rs2238691
rs2238691
3 19 45675785 intron variant G/A snv 0.17 0.700 1.000 1 2019 2019
dbSNP: rs35560038
rs35560038
1 19 45671788 intron variant A/T snv 0.24 0.700 1.000 1 2017 2017