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: rs11720523
rs11720523
1 3 71496019 intron variant C/A snv 0.35 0.700 1.000 2 2018 2018
dbSNP: rs6779258
rs6779258
2 1.000 0.040 3 71500488 intron variant T/C snv 0.35 0.700 1.000 2 2019 2019
dbSNP: rs55736314
rs55736314
1 3 71537142 intron variant C/G snv 0.29 0.700 1.000 1 2017 2017
dbSNP: rs56151722
rs56151722
1 3 71433689 intron variant A/G snv 0.56 0.700 1.000 1 2018 2018