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: rs363276
rs363276
1 1.000 0.040 10 117274298 intron variant T/C;G snv 0.020 1.000 2 2014 2018
dbSNP: rs10144436
rs10144436
1 1.000 0.040 14 95090065 3 prime UTR variant C/A snv 2.9E-02 0.010 1.000 1 2015 2015
dbSNP: rs10170218
rs10170218
1 1.000 0.040 2 187949717 intron variant A/C snv 0.25 0.700 1.000 1 2013 2013
dbSNP: rs1033962
rs1033962
1 1.000 0.040 10 24927877 intron variant C/T snv 0.33 0.700 1.000 1 2015 2015
dbSNP: rs10744891
rs10744891
1 1.000 0.040 12 117284536 intron variant G/T snv 0.41 0.010 1.000 1 2017 2017
dbSNP: rs10852889
rs10852889
1 1.000 0.040 17 6997526 intron variant C/A;G;T snv 0.010 1.000 1 2015 2015
dbSNP: rs11599164
rs11599164
1 1.000 0.040 10 60072226 missense variant G/T snv 7.2E-02 7.3E-02 0.010 1.000 1 2013 2013
dbSNP: rs1187327
rs1187327
1 1.000 0.040 9 84673625 intron variant T/C snv 0.50 0.010 1.000 1 2017 2017
dbSNP: rs12458282
rs12458282
MBP
1 1.000 0.040 18 77061897 intron variant T/C snv 0.24 0.010 1.000 1 2019 2019
dbSNP: rs12898919
rs12898919
1 1.000 0.040 15 78588235 intron variant G/C snv 3.1E-02 0.010 1.000 1 2015 2015
dbSNP: rs1374141592
rs1374141592
1 1.000 0.040 5 180630561 missense variant C/T snv 7.0E-06 0.010 1.000 1 2016 2016
dbSNP: rs159572
rs159572
1 1.000 0.040 5 56211219 intron variant A/C snv 0.37 0.700 1.000 1 2016 2016
dbSNP: rs16904179
rs16904179
1 1.000 0.040 8 129946705 intron variant G/A snv 6.2E-02 0.800 1.000 1 2013 2013
dbSNP: rs17208576
rs17208576
1 1.000 0.040 10 60074815 synonymous variant G/A snv 7.2E-02 7.3E-02 0.010 1.000 1 2013 2013
dbSNP: rs1990322
rs1990322
1 1.000 0.040 12 2651804 intron variant G/A snv 0.69 0.57 0.010 1.000 1 2018 2018
dbSNP: rs2074621
rs2074621
1 1.000 0.040 19 15179601 non coding transcript exon variant G/A snv 0.67 0.010 1.000 1 2020 2020
dbSNP: rs2075652
rs2075652
1 1.000 0.040 11 113424176 intron variant G/A snv 4.2E-02 0.010 1.000 1 2015 2015
dbSNP: rs2108977
rs2108977
1 1.000 0.040 11 18019049 3 prime UTR variant T/C snv 0.47 0.010 1.000 1 2012 2012
dbSNP: rs2251177
rs2251177
1 1.000 0.040 3 114139503 missense variant C/A;T snv 8.0E-06; 0.99 0.010 1.000 1 2014 2014
dbSNP: rs2267715
rs2267715
1 1.000 0.040 7 30676471 intron variant G/A;C snv 0.010 1.000 1 2020 2020
dbSNP: rs2400207
rs2400207
1 1.000 0.040 5 146000534 intron variant A/G snv 0.56 0.010 1.000 1 2018 2018
dbSNP: rs263232
rs263232
1 1.000 0.040 8 130795923 intron variant C/A snv 6.7E-02 0.800 1.000 1 2014 2014
dbSNP: rs28932171
rs28932171
1 1.000 0.040 10 60071532 missense variant T/C snv 7.2E-02 7.3E-02 0.010 1.000 1 2013 2013
dbSNP: rs3100127
rs3100127
1 1.000 0.040 1 202191842 upstream gene variant C/A;T snv 0.700 1.000 1 2015 2015
dbSNP: rs356195
rs356195
1 1.000 0.040 4 89762017 intron variant T/C snv 0.81 0.010 1.000 1 2015 2015