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: rs10475598
rs10475598
1 5 174221435 intron variant T/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs1149530
rs1149530
1 7 16808751 intron variant T/C snv 0.91 0.700 1.000 1 2018 2018
dbSNP: rs117328143
rs117328143
1 6 137333172 regulatory region variant C/A snv 2.0E-02 0.700 1.000 1 2019 2019
dbSNP: rs17518584
rs17518584
8 0.827 0.160 3 85555773 intron variant C/T snv 0.50 0.700 1.000 1 2016 2016
dbSNP: rs187701342
rs187701342
1 15 81618804 intron variant C/T snv 3.3E-02 0.700 1.000 1 2019 2019
dbSNP: rs2118666
rs2118666
1 2 222235804 intron variant G/T snv 0.44 0.700 1.000 1 2016 2016
dbSNP: rs2199301
rs2199301
1 18 31330652 intron variant A/G snv 0.42 0.700 1.000 1 2014 2014
dbSNP: rs2353010
rs2353010
1 5 1912366 intergenic variant C/T snv 0.20 0.700 1.000 1 2019 2019
dbSNP: rs2734839
rs2734839
2 1.000 0.040 11 113415768 intron variant C/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs3752060
rs3752060
1 18 41565183 intron variant G/T snv 3.2E-02 0.700 1.000 1 2019 2019
dbSNP: rs58366817
rs58366817
1 12 47540749 intergenic variant T/C snv 0.13 0.700 1.000 1 2019 2019
dbSNP: rs6051520
rs6051520
1 20 371300 intron variant T/G snv 0.33 0.700 1.000 1 2011 2011
dbSNP: rs664154
rs664154
1 6 18991328 intergenic variant C/T snv 0.31 0.700 1.000 1 2016 2016
dbSNP: rs71399907
rs71399907
1 16 69999056 intron variant C/T snv 1.8E-02 0.700 1.000 1 2019 2019
dbSNP: rs7219585
rs7219585
1 17 74272069 upstream gene variant A/G;T snv 0.700 1.000 1 2011 2011