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: rs2069416
rs2069416
3 0.925 0.040 9 22010005 intron variant T/A;G snv 0.700 1.000 2 2011 2013
dbSNP: rs3217992
rs3217992
22 0.683 0.480 9 22003224 3 prime UTR variant C/T snv 0.32 0.700 1.000 2 2011 2013
dbSNP: rs1063192
rs1063192
24 0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs2069418
rs2069418
2 1.000 0.040 9 22009699 intron variant G/C snv 0.70 0.700 1.000 1 2011 2011