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: rs12507127
rs12507127
1 4 7918540 intron variant A/C snv 0.40 0.700 1.000 1 2018 2018
dbSNP: rs28500712
rs28500712
2 1.000 0.040 4 7894486 intron variant A/C;G snv 0.700 1.000 1 2018 2018
dbSNP: rs28520091
rs28520091
2 1.000 0.040 4 7844513 intron variant C/A;G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs28649910
rs28649910
1 4 7859556 intron variant A/C;G snv 0.700 1.000 1 2018 2018
dbSNP: rs28795989
rs28795989
2 1.000 0.040 4 7889818 intron variant A/C;G snv 0.700 1.000 1 2017 2017
dbSNP: rs62289359
rs62289359
1 4 7895441 intron variant C/T snv 0.35 0.700 1.000 1 2018 2018
dbSNP: rs6816389
rs6816389
1 4 7862730 intron variant T/C snv 0.31 0.700 1.000 1 2018 2018