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: rs1057521927
rs1057521927
2 1.000 1 151017860 missense variant G/A snv 0.800 1.000 3 2015 2017
dbSNP: rs773618224
rs773618224
2 1.000 1 151018650 missense variant G/A snv 5.2E-05 2.8E-05 0.800 1.000 3 2015 2017
dbSNP: rs1085308033
rs1085308033
1 1.000 1 151018494 missense variant C/A snv 0.800 0
dbSNP: rs752599948
rs752599948
1 1.000 1 151028900 missense variant C/T snv 4.0E-06 0.800 0
dbSNP: rs767769359
rs767769359
2 1.000 1 151024658 missense variant G/A;C;T snv 2.0E-05; 8.0E-06 0.800 0
dbSNP: rs200618384
rs200618384
2 1.000 1 151024795 stop gained G/C;T snv 0.700 0
dbSNP: rs886039608
rs886039608
1 1.000 1 151025513 splice acceptor variant A/G snv 0.700 0