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: rs10211774
rs10211774
1 20 4172971 intron variant G/A;C;T snv 0.700 1.000 1 2016 2016
dbSNP: rs1051904
rs1051904
1 20 4182655 synonymous variant A/G snv 0.61 0.60 0.700 1.000 1 2016 2016
dbSNP: rs13038292
rs13038292
1 20 4157982 intron variant C/G snv 4.6E-02 0.700 1.000 1 2016 2016
dbSNP: rs13043612
rs13043612
1 20 4151717 intron variant C/G snv 0.24 0.700 1.000 1 2016 2016
dbSNP: rs1741314
rs1741314
1 20 4174546 intron variant T/C snv 0.57 0.700 1.000 1 2016 2016
dbSNP: rs1765003
rs1765003
1 20 4155202 intron variant G/A snv 0.30 0.700 1.000 1 2016 2016
dbSNP: rs6084646
rs6084646
1 20 4144492 intron variant C/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs6515865
rs6515865
1 20 4145672 intron variant T/C snv 0.37 0.700 1.000 1 2016 2016