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: rs17020055
rs17020055
1 1.000 0.040 1 107793911 intron variant A/C snv 0.11 0.800 1.000 2 2012 2016
dbSNP: rs4915077
rs4915077
1 1.000 0.040 1 107823394 intron variant T/C snv 9.0E-02 0.800 1.000 1 2012 2012
dbSNP: rs17019823
rs17019823
1 1.000 0.040 1 107727331 intron variant A/C snv 9.6E-02 0.700 1.000 1 2012 2012
dbSNP: rs17020088
rs17020088
1 1.000 0.040 1 107809190 intron variant T/C snv 0.15 0.700 1.000 1 2012 2012
dbSNP: rs17020139
rs17020139
1 1.000 0.040 1 107826861 intron variant G/A snv 9.0E-02 0.700 1.000 1 2019 2019
dbSNP: rs4915076
rs4915076
3 0.882 0.080 1 107816883 intron variant T/C snv 9.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs78495697
rs78495697
1 1.000 0.040 1 107813097 intron variant C/T snv 9.2E-02 0.700 1.000 1 2018 2018