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: rs60239918
rs60239918
1 1.000 0.080 19 45077114 intron variant C/T snv 4.2E-02 0.700 1.000 2 2018 2019
dbSNP: rs183321458
rs183321458
1 1.000 0.080 19 45077818 intron variant G/A snv 2.4E-03 0.700 1.000 1 2019 2019
dbSNP: rs7251911
rs7251911
1 1.000 0.080 19 45079144 intron variant C/G snv 0.16 0.700 1.000 1 2018 2018
dbSNP: rs78620885
rs78620885
1 1.000 0.080 19 45087826 intron variant C/T snv 3.1E-02 0.700 1.000 1 2018 2018
dbSNP: rs8100183
rs8100183
1 1.000 0.080 19 45081434 intron variant C/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs9653111
rs9653111
1 1.000 0.080 19 45089217 intron variant C/T snv 9.9E-02 0.700 1.000 1 2019 2019