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: rs11067815
rs11067815
1 1.000 0.040 12 115876463 intron variant A/T snv 0.14 0.700 1.000 1 2013 2013
dbSNP: rs4767382
rs4767382
1 1.000 0.040 12 115884185 intron variant A/G snv 0.32 0.700 1.000 1 2013 2013
dbSNP: rs7964653
rs7964653
1 1.000 0.040 12 115875621 intron variant A/G snv 0.21 0.700 1.000 1 2013 2013
dbSNP: rs7967915
rs7967915
1 1.000 0.040 12 115875910 intron variant T/C snv 0.23 0.700 1.000 1 2013 2013