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: rs2038123
rs2038123
2 20 34108259 non coding transcript exon variant A/G snv 8.6E-02 0.700 1.000 1 2010 2010
dbSNP: rs2268081
rs2268081
2 20 34016024 intron variant A/C snv 8.7E-02 0.700 1.000 1 2010 2010
dbSNP: rs2268083
rs2268083
2 20 34038129 intron variant C/T snv 4.6E-02 0.700 1.000 1 2010 2010
dbSNP: rs2268087
rs2268087
2 20 34061179 intron variant G/A;T snv 0.700 1.000 1 2010 2010
dbSNP: rs2284380
rs2284380
2 20 34006908 intron variant C/A;T snv 8.7E-02 0.700 1.000 1 2010 2010
dbSNP: rs2284385
rs2284385
2 20 34049195 intron variant A/G snv 6.0E-02 4.4E-02 0.700 1.000 1 2010 2010
dbSNP: rs2284390
rs2284390
2 20 34069784 intron variant G/A snv 0.10 0.700 1.000 1 2010 2010
dbSNP: rs2284391
rs2284391
2 20 34074145 intron variant T/A snv 8.6E-02 0.700 1.000 1 2010 2010
dbSNP: rs2300202
rs2300202
2 20 34000876 intron variant G/T snv 8.7E-02 0.700 1.000 1 2010 2010
dbSNP: rs6088387
rs6088387
2 20 34041516 intron variant G/T snv 8.7E-02 0.700 1.000 1 2010 2010
dbSNP: rs6088389
rs6088389
2 20 34054109 intron variant G/T snv 0.10 0.700 1.000 1 2010 2010
dbSNP: rs6088393
rs6088393
2 20 34086691 intron variant G/A snv 4.4E-02 0.700 1.000 1 2010 2010
dbSNP: rs6088397
rs6088397
2 20 34094306 intron variant A/G snv 9.1E-02 0.700 1.000 1 2010 2010
dbSNP: rs6088398
rs6088398
2 20 34102714 intron variant G/C snv 8.6E-02 0.700 1.000 1 2010 2010
dbSNP: rs6119446
rs6119446
2 20 34071524 intron variant C/G snv 8.6E-02 0.700 1.000 1 2010 2010
dbSNP: rs9974023
rs9974023
2 20 34051022 intron variant A/C;G snv 0.700 1.000 1 2010 2010