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: rs140291094
rs140291094
11 0.742 0.320 12 57244322 missense variant C/G snv 9.1E-05 3.8E-04 0.010 1.000 1 2017 2017
dbSNP: rs2272515
rs2272515
3 0.882 0.080 3 120416036 intron variant T/C snv 0.36 0.34 0.010 1.000 1 2019 2019