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: rs6091540
rs6091540
2 20 52471323 intron variant C/T snv 0.26 0.700 1.000 5 2015 2018
dbSNP: rs16996700
rs16996700
3 20 52365406 intron variant T/C snv 0.29 0.700 1.000 1 2018 2018
dbSNP: rs17806224
rs17806224
1 20 52449315 intron variant G/A snv 0.13 0.700 1.000 1 2019 2019
dbSNP: rs35388084
rs35388084
1 20 52343951 intron variant G/A snv 0.15 0.700 1.000 1 2019 2019
dbSNP: rs66460909
rs66460909
1 20 52578848 intron variant G/A snv 0.14 0.700 1.000 1 2019 2019