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: rs9922678
rs9922678
1 1.000 0.040 16 9852462 intron variant G/A;C snv 0.700 1.000 4 2014 2019
dbSNP: rs7191183
rs7191183
2 1.000 0.040 16 9806200 intron variant T/C snv 0.35 0.700 1.000 3 2017 2019
dbSNP: rs117304774
rs117304774
2 1.000 0.040 16 10057377 intron variant G/A snv 8.2E-03 0.700 1.000 1 2019 2019