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: rs5998500
rs5998500
1 22 32463715 intron variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs738263
rs738263
2 22 32466395 upstream gene variant G/A snv 0.44 0.700 1.000 1 2012 2012
dbSNP: rs8135723
rs8135723
1 22 32464263 intron variant T/C snv 0.41 0.700 1.000 1 2012 2012
dbSNP: rs9606957
rs9606957
2 22 32465096 upstream gene variant T/C;G snv 0.700 1.000 1 2012 2012
dbSNP: rs9609562
rs9609562
1 22 32464805 upstream gene variant C/T snv 0.25 0.700 1.000 1 2012 2012