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: rs12105918
rs12105918
1 1.000 0.120 2 144450626 intron variant T/C snv 6.1E-02 0.800 1.000 2 2013 2017
dbSNP: rs2121266
rs2121266
1 1.000 0.120 2 46308785 intron variant C/A snv 0.61 0.800 1.000 2 2011 2019
dbSNP: rs72858496
rs72858496
1 1.000 0.120 2 144452349 intron variant C/T snv 5.9E-02 0.800 1.000 2 2013 2015
dbSNP: rs10054504
rs10054504
1 1.000 0.120 5 32000377 intron variant T/A;C snv 0.800 1.000 1 2013 2013
dbSNP: rs10211665
rs10211665
1 1.000 0.120 2 46298957 intron variant T/C snv 0.58 0.700 1.000 1 2011 2011
dbSNP: rs10484683
rs10484683
1 1.000 0.120 6 147830941 intron variant A/G snv 0.18 0.700 1.000 1 2019 2019
dbSNP: rs1057519973
rs1057519973
1 1.000 0.120 8 73946733 missense variant T/A;G snv 0.700 1.000 1 2016 2016
dbSNP: rs1057519974
rs1057519974
1 1.000 0.120 8 73946734 missense variant A/T snv 0.700 1.000 1 2016 2016
dbSNP: rs11125068
rs11125068
1 1.000 0.120 2 46300677 intron variant A/G snv 0.62 0.700 1.000 1 2011 2011
dbSNP: rs11263654
rs11263654
1 1.000 0.120 11 69423355 upstream gene variant C/T snv 0.11 0.700 1.000 1 2015 2015
dbSNP: rs11637556
rs11637556
1 1.000 0.120 15 66436613 intron variant A/C;G snv 0.700 1.000 1 2017 2017
dbSNP: rs11684885
rs11684885
1 1.000 0.120 2 46306413 intron variant T/C;G snv 0.700 1.000 1 2011 2011
dbSNP: rs12105521
rs12105521
1 1.000 0.120 2 144450769 intron variant G/A;T snv 0.700 1.000 1 2013 2013
dbSNP: rs13027293
rs13027293
1 1.000 0.120 2 119243542 intron variant G/T snv 0.33 0.700 1.000 1 2019 2019
dbSNP: rs13376700
rs13376700
1 1.000 0.120 1 51011971 intergenic variant T/A snv 0.48 0.700 1.000 1 2017 2017
dbSNP: rs13401103
rs13401103
1 1.000 0.120 2 144441056 intron variant G/A;T snv 0.700 1.000 1 2013 2013
dbSNP: rs1492078
rs1492078
1 1.000 0.120 3 148697390 upstream gene variant T/C snv 0.50 0.010 1.000 1 2015 2015
dbSNP: rs17034950
rs17034950
1 1.000 0.120 2 46311655 intron variant G/A snv 0.25 0.700 1.000 1 2011 2011
dbSNP: rs1800645
rs1800645
1 1.000 0.120 8 90083245 intron variant A/G;T snv 0.010 1.000 1 2012 2012
dbSNP: rs1867784
rs1867784
1 1.000 0.120 2 46307081 intron variant T/C snv 0.40 0.700 1.000 1 2011 2011
dbSNP: rs1867785
rs1867785
1 1.000 0.120 2 46307199 intron variant A/G snv 0.52 0.700 1.000 1 2011 2011
dbSNP: rs1867787
rs1867787
1 1.000 0.120 2 46298252 intron variant G/C;T snv 0.700 1.000 1 2011 2011
dbSNP: rs1944129
rs1944129
1 1.000 0.120 11 69639167 upstream gene variant C/G;T snv 0.010 1.000 1 2017 2017
dbSNP: rs2034327
rs2034327
1 1.000 0.120 2 46321901 intron variant G/C snv 0.59 0.700 1.000 1 2011 2011
dbSNP: rs2044456
rs2044456
1 1.000 0.120 2 46319177 intron variant A/G snv 0.26 0.700 1.000 1 2011 2011