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: rs1535
rs1535
24 0.752 0.240 11 61830500 intron variant A/G snv 0.31 0.700 1.000 1 2019 2019
dbSNP: rs174564
rs174564
4 1.000 0.080 11 61820833 intron variant A/G snv 0.30 0.700 1.000 1 2019 2019
dbSNP: rs174567
rs174567
4 1.000 0.080 11 61825533 intron variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs174574
rs174574
7 1.000 0.080 11 61832870 intron variant A/C snv 0.55 0.700 1.000 1 2019 2019
dbSNP: rs174580
rs174580
4 1.000 0.080 11 61839170 intron variant A/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs174601
rs174601
12 0.925 0.080 11 61855668 non coding transcript exon variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs2072114
rs2072114
4 1.000 0.080 11 61837743 intron variant A/G snv 0.19 0.16 0.700 1.000 1 2019 2019
dbSNP: rs28456
rs28456
5 0.925 0.120 11 61822009 intron variant A/C;G snv 0.700 1.000 1 2019 2019