Source: ALL
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: rs10093796
rs10093796
GML
1 8 142897008 intron variant T/C snv 0.67 0.700 1.000 1 2018 2018
dbSNP: rs10841753
rs10841753
SLCO1B1
3 0.925 0.080 12 21168436 intron variant T/C snv 0.19 0.700 1.000 1 2017 2017
dbSNP: rs10953024
rs10953024
CDK14
2 7 90874752 intron variant T/C snv 0.12 0.700 1.000 1 2017 2017
dbSNP: rs12586722
rs12586722 		2 1.000 14 70423423 downstream gene variant G/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs17277546
rs17277546
TRIM4
4 7 99891948 3 prime UTR variant G/A snv 3.1E-02 0.700 1.000 1 2018 2018
dbSNP: rs2899472
rs2899472
CYP19A1 ; MIR4713HG
2 1.000 0.080 15 51223858 intron variant C/A snv 0.17 0.700 1.000 1 2018 2018
dbSNP: rs727479
rs727479
CYP19A1 ; MIR4713 ; MIR4713HG
10 0.790 0.240 15 51242350 intron variant C/A;T snv 0.700 1.000 1 2018 2018