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: rs1501299
rs1501299
52 0.597 0.720 3 186853334 intron variant G/C;T snv 0.010 1.000 1 2013 2013
dbSNP: rs2241767
rs2241767
10 0.763 0.440 3 186853407 intron variant A/G snv 0.10 0.010 1.000 1 2013 2013
dbSNP: rs80356814
rs80356814
15 0.732 0.320 1 156138697 synonymous variant C/T snv 8.0E-06 0.010 1.000 1 2011 2011
dbSNP: rs822396
rs822396
16 0.732 0.400 3 186849088 intron variant G/A snv 0.81 0.010 1.000 1 2013 2013