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: rs1217691063
rs1217691063
614 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 0.010 1.000 1 2012 2012
dbSNP: rs3736228
rs3736228
13 0.752 0.400 11 68433827 missense variant C/T snv 0.13 0.11 0.010 1.000 1 2014 2014
dbSNP: rs3794060
rs3794060
2 0.925 0.160 11 71476633 3 prime UTR variant C/T snv 0.53 0.010 1.000 1 2018 2018
dbSNP: rs4944957
rs4944957
2 1.000 0.080 11 71456989 intron variant A/G snv 0.62 0.010 1.000 1 2018 2018