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: rs1499428
rs1499428
LOC105375716 ; LOC105375717
1 1.000 0.080 8 117287936 intron variant C/G snv 0.30 0.700 1.000 1 2018 2018
dbSNP: rs186544372
rs186544372
LOC107986195
1 1.000 0.080 4 148995525 intron variant T/A snv 1.4E-02 0.700 1.000 1 2018 2018
dbSNP: rs188172955
rs188172955 		1 1.000 0.080 10 37047661 intergenic variant G/A snv 8.8E-04 0.700 1.000 1 2018 2018
dbSNP: rs74835610
rs74835610 		1 1.000 0.080 1 165171177 intergenic variant T/G snv 1.2E-02 0.700 1.000 1 2018 2018