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: rs17087335
rs17087335
1 1.000 0.040 4 56972417 intron variant G/T snv 0.20 0.700 1.000 1 2015 2015
dbSNP: rs57265257
rs57265257
2 1.000 0.040 4 56973114 intron variant A/T snv 0.22 0.20 0.700 1.000 1 2018 2018
dbSNP: rs72627509
rs72627509
1 1.000 0.040 4 56972885 intron variant C/G snv 0.18 0.700 1.000 1 2017 2017