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: rs1049353
rs1049353
26 0.657 0.464 6 88143916 synonymous variant C/T snp 0.21 0.20 0.010 1.000 1 2004 2004
dbSNP: rs1390938
rs1390938
3 0.878 0.143 8 20179202 missense variant A/G snp 0.71 0.77 0.010 1.000 1 2017 2017
dbSNP: rs1800566
rs1800566
41 0.605 0.571 16 69711242 missense variant G/A snp 0.25 0.21 0.010 < 0.001 1 2004 2004
dbSNP: rs532358159
rs532358159
30 0.634 0.536 16 69711143 missense variant G/A snp 4.0E-06 0.010 < 0.001 1 2004 2004