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: rs111873142
rs111873142
1 17 82910808 intron variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs112912841
rs112912841
LPP
1 3 188269895 intron variant A/G snv 0.12 0.700 1.000 1 2019 2019
dbSNP: rs116461311
rs116461311
1 4 20329377 intron variant A/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs117023642
rs117023642
2 8 20981609 intron variant C/G snv 1.6E-02 0.700 1.000 1 2019 2019
dbSNP: rs11788387
rs11788387
2 9 81855961 regulatory region variant G/T snv 0.14 0.700 1.000 1 2019 2019
dbSNP: rs140162370
rs140162370
1 18 23391045 intron variant G/C snv 2.7E-02 0.700 1.000 1 2019 2019
dbSNP: rs149014416
rs149014416
2 8 29812253 downstream gene variant G/- delins 1.5E-02 0.700 1.000 1 2017 2017
dbSNP: rs1558001
rs1558001
2 7 81777764 intergenic variant T/C snv 0.63 0.700 1.000 1 2017 2017
dbSNP: rs1877720
rs1877720
1 1 48358735 intron variant C/T snv 7.1E-02 0.700 1.000 1 2019 2019
dbSNP: rs2001841
rs2001841
1 3 61513935 intergenic variant G/A snv 0.34 0.700 1.000 1 2019 2019
dbSNP: rs2146858
rs2146858
1 14 57067427 intron variant C/A;T snv 0.44 0.700 1.000 1 2019 2019
dbSNP: rs34635471
rs34635471
1 3 170594457 intron variant AA/- del 5.3E-02 0.700 1.000 1 2019 2019
dbSNP: rs35113467
rs35113467
1 10 126538306 intron variant T/C snv 0.18 0.700 1.000 1 2019 2019
dbSNP: rs3777722
rs3777722
1 6 166938616 missense variant C/A;G;T snv 0.18; 4.1E-06; 6.6E-05 0.700 1.000 1 2015 2015
dbSNP: rs480745
rs480745
1 1 82804287 intron variant G/A snv 6.4E-02 0.700 1.000 1 2015 2015
dbSNP: rs539974331
rs539974331
1 1 182336514 downstream gene variant AA/-;A;AAA delins 1.6E-02 0.700 1.000 1 2019 2019
dbSNP: rs61953951
rs61953951
1 13 31486393 upstream gene variant G/A snv 8.9E-02 0.700 1.000 1 2019 2019
dbSNP: rs687184
rs687184
1 9 22725625 intron variant G/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs72545460
rs72545460
1 20 2163705 intron variant -/C ins 0.700 1.000 1 2019 2019
dbSNP: rs737263
rs737263
1 22 44244728 3 prime UTR variant G/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs73814923
rs73814923
1 3 11608090 intron variant C/A;T snv 0.700 1.000 1 2019 2019