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: rs34305371
rs34305371
1 1 72267927 intron variant G/A snv 6.6E-02 0.700 1.000 4 2017 2019
dbSNP: rs17589603
rs17589603
1 1 72167202 intron variant A/G snv 7.4E-02 0.700 1.000 3 2018 2019
dbSNP: rs12128707
rs12128707
1 1 72122436 intron variant A/G snv 0.21 0.700 1.000 2 2018 2019
dbSNP: rs3128341
rs3128341
2 1 72284165 intron variant T/C snv 0.82 0.700 1.000 2 2018 2019
dbSNP: rs1026997
rs1026997
1 1 72050604 intron variant T/C snv 0.45 0.700 1.000 1 2019 2019
dbSNP: rs114030538
rs114030538
1 1 72122975 intron variant T/C snv 4.1E-02 0.700 1.000 1 2018 2018
dbSNP: rs1157072
rs1157072
1 1 72169229 intron variant A/G snv 3.6E-02 0.700 1.000 1 2019 2019
dbSNP: rs11576565
rs11576565
1 1 71649104 intron variant G/A snv 0.36 0.700 1.000 1 2019 2019
dbSNP: rs11587895
rs11587895
1 1 72146932 intron variant T/C snv 0.22 0.700 1.000 1 2018 2018
dbSNP: rs12124523
rs12124523
2 1.000 0.040 1 72155780 intron variant C/T snv 7.0E-02 0.700 1.000 1 2019 2019
dbSNP: rs12125471
rs12125471
1 1 71441857 intron variant C/T snv 7.7E-02 0.700 1.000 1 2019 2019
dbSNP: rs12130762
rs12130762
1 1 71687405 intron variant G/A snv 6.5E-02 0.700 1.000 1 2019 2019
dbSNP: rs12133604
rs12133604
1 1 72145196 intron variant G/T snv 0.41 0.700 1.000 1 2019 2019
dbSNP: rs12137231
rs12137231
1 1 72269775 intron variant T/C snv 0.35 0.700 1.000 1 2019 2019
dbSNP: rs12139692
rs12139692
1 1 71995699 intron variant C/T snv 7.4E-02 0.700 1.000 1 2019 2019
dbSNP: rs12143094
rs12143094
1 1 71639693 intron variant G/C snv 3.9E-02 0.700 1.000 1 2019 2019
dbSNP: rs12564885
rs12564885
1 1 71597627 intron variant A/T snv 0.24 0.700 1.000 1 2018 2018
dbSNP: rs1486091
rs1486091
1 1 72105681 intron variant C/T snv 0.55 0.700 1.000 1 2018 2018
dbSNP: rs1620977
rs1620977
3 1.000 0.040 1 72263459 intron variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs1870676
rs1870676
1 1 72279313 intron variant T/C snv 0.48 0.700 1.000 1 2018 2018
dbSNP: rs2016698
rs2016698
1 1 72096795 intron variant G/A snv 0.23 0.700 1.000 1 2019 2019
dbSNP: rs2821260
rs2821260
1 1 72088410 intron variant C/T snv 0.59 0.700 1.000 1 2019 2019
dbSNP: rs4348675
rs4348675
1 1 72050034 intron variant T/C snv 9.0E-02 0.700 1.000 1 2018 2018
dbSNP: rs66495454
rs66495454
1 1 72282884 upstream gene variant -/TCC;TCCT ins 0.28 0.700 1.000 1 2017 2017
dbSNP: rs67474621
rs67474621
1 1 72112267 intron variant A/C;T snv 0.700 1.000 1 2018 2018