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: rs1057519816
rs1057519816
14 0.763 0.200 17 39711955 missense variant C/A;T snv 0.010 1.000 1 2016 2016
dbSNP: rs1131692237
rs1131692237
2 1.000 0.040 17 39725161 missense variant T/G snv 0.010 1.000 1 2018 2018
dbSNP: rs1136201
rs1136201
34 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 0.010 < 0.001 1 2008 2008
dbSNP: rs1308088661
rs1308088661
2 17 39727880 missense variant G/A snv 4.0E-06 0.010 1.000 1 2019 2019
dbSNP: rs61552325
rs61552325
5 0.882 0.080 17 39727784 missense variant C/G snv 0.010 1.000 1 2017 2017
dbSNP: rs759478535
rs759478535
6 0.851 0.080 17 39708351 missense variant A/G snv 6.8E-05 4.2E-05 0.010 1.000 1 2016 2016
dbSNP: rs767151455
rs767151455
4 0.925 0.080 17 39708379 missense variant C/T snv 8.0E-06 0.010 1.000 1 2018 2018