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: rs10929757
rs10929757
2 1.000 2 11562535 missense variant A/C snv 0.54 0.44 0.700 1.000 1 2018 2018
dbSNP: rs148143917
rs148143917
2 1.000 2 11524625 intron variant A/C snv 9.8E-03 0.700 1.000 1 2018 2018
dbSNP: rs35417544
rs35417544
2 1.000 2 11540277 intron variant C/T snv 0.59 0.700 1.000 1 2019 2019