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: rs1448903
rs1448903
1 2 206444237 intron variant A/G snv 6.1E-02 0.700 1.000 3 2018 2019
dbSNP: rs13429599
rs13429599
1 2 206548901 intron variant G/A snv 0.25 0.700 1.000 1 2019 2019
dbSNP: rs143219430
rs143219430
1 2 206527534 intron variant A/C snv 1.3E-02 0.700 1.000 1 2018 2018
dbSNP: rs1921673
rs1921673
1 2 206459558 intron variant A/G snv 0.70 0.700 1.000 1 2018 2018
dbSNP: rs33998651
rs33998651
1 2 206517977 intron variant G/A snv 1.8E-02 0.700 1.000 1 2018 2018