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: rs71352238
rs71352238
1 1.000 0.080 19 44891079 intron variant T/C snv 0.10 0.700 1.000 1 2019 2019
dbSNP: rs741780
rs741780
1 1.000 0.080 19 44901174 intron variant T/C snv 0.47 0.52 0.700 1.000 1 2013 2013
dbSNP: rs76692773
rs76692773
1 1.000 0.080 19 44890954 intron variant C/T snv 7.5E-02 0.700 1.000 1 2019 2019
dbSNP: rs77301115
rs77301115
2 1.000 0.080 19 44893716 intron variant G/A snv 2.8E-02 0.700 1.000 1 2019 2019