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: rs10138860
rs10138860
1 1.000 0.040 14 56506061 intron variant T/C snv 0.21 0.700 1.000 1 2017 2017
dbSNP: rs11621999
rs11621999
1 1.000 0.040 14 56507773 intron variant A/G snv 0.11 0.700 1.000 1 2017 2017
dbSNP: rs12893499
rs12893499
1 1.000 0.040 14 56513226 intron variant A/C snv 0.14 0.700 1.000 1 2017 2017
dbSNP: rs1959060
rs1959060
1 1.000 0.040 14 56505747 intron variant A/G snv 0.47 0.700 1.000 1 2017 2017
dbSNP: rs4274344
rs4274344
1 1.000 0.040 14 56505920 intron variant C/T snv 0.47 0.700 1.000 1 2017 2017
dbSNP: rs7156058
rs7156058
1 1.000 0.040 14 56505354 intron variant G/T snv 0.29 0.700 1.000 1 2017 2017
dbSNP: rs8012512
rs8012512
1 1.000 0.040 14 56504660 intron variant A/G;T snv 0.700 1.000 1 2017 2017