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: rs318240758
rs318240758
1 1.000 0.080 X 153963263 missense variant C/T snv 0.800 1.000 1 2012 2012
dbSNP: rs188675529
rs188675529
11 0.827 0.240 16 67842794 missense variant C/G;T snv 1.6E-03 6.0E-04 0.700 0
dbSNP: rs397515485
rs397515485
1 1.000 0.080 X 153964283 missense variant G/A;C snv 0.700 0
dbSNP: rs397515486
rs397515486
2 0.925 0.200 X 153964702 missense variant G/A snv 0.700 0
dbSNP: rs397515487
rs397515487
1 1.000 0.080 X 153964703 missense variant C/T snv 0.700 0
dbSNP: rs398122908
rs398122908
1 1.000 0.080 X 153971810 5 prime UTR variant A/G snv 0.700 0
dbSNP: rs869312686
rs869312686
5 0.882 0.120 X 153952053 missense variant G/C;T snv 0.700 0