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: rs56150095
rs56150095
1 7 72294084 intron variant C/A snv 0.47 0.700 1.000 2 2018 2018
dbSNP: rs10227076
rs10227076
1 7 72398837 intron variant G/A snv 0.54 0.700 1.000 1 2018 2018
dbSNP: rs2944839
rs2944839
1 7 72305718 intron variant C/T snv 0.46 0.700 1.000 1 2019 2019
dbSNP: rs34711194
rs34711194
1 7 72224689 intron variant G/A snv 0.20 0.700 1.000 1 2018 2018
dbSNP: rs35417702
rs35417702
2 1.000 0.040 7 72274931 intron variant C/T snv 0.46 0.700 1.000 1 2019 2019
dbSNP: rs55841409
rs55841409
1 7 72342201 intron variant G/A snv 0.24 0.700 1.000 1 2018 2018
dbSNP: rs7783256
rs7783256
1 7 72269589 intron variant G/C;T snv 0.700 1.000 1 2019 2019
dbSNP: rs7808347
rs7808347
1 7 72227405 intron variant T/C snv 0.53 0.700 1.000 1 2018 2018
dbSNP: rs79527984
rs79527984
1 7 72387188 intron variant G/A snv 0.36 0.700 1.000 1 2019 2019
dbSNP: rs865225
rs865225
1 7 72115265 intron variant G/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs9638655
rs9638655
1 7 72372316 intron variant A/G;T snv 0.700 1.000 1 2018 2018