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: rs1041867
rs1041867
1 1.000 0.080 21 33354946 intron variant T/G snv 0.48 0.010 1.000 1 2018 2018
dbSNP: rs12626750
rs12626750
1 1.000 0.080 21 33326080 intron variant C/A snv 0.24 0.010 1.000 1 2018 2018
dbSNP: rs2257167
rs2257167
7 0.807 0.200 21 33343393 missense variant G/C snv 0.18 0.16 0.010 1.000 1 2003 2003
dbSNP: rs914142
rs914142
1 1.000 0.080 21 33353501 intron variant G/A;T snv 0.010 1.000 1 2018 2018