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: rs8042149
rs8042149
3 0.882 0.160 15 60832754 intron variant T/G snv 0.44 0.720 1.000 3 2013 2019
dbSNP: rs4775301
rs4775301
2 0.925 0.040 15 60834660 intron variant T/C;G snv 0.700 1.000 1 2013 2013
dbSNP: rs8024133
rs8024133
2 0.925 0.040 15 60838440 intron variant C/T snv 0.42 0.700 1.000 1 2013 2013
dbSNP: rs8041061
rs8041061
2 0.925 0.040 15 60832639 intron variant G/T snv 0.39 0.700 1.000 1 2013 2013