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: rs6674176
rs6674176
1 1 43914285 3 prime UTR variant G/A snv 0.64 0.700 1.000 2 2017 2019
dbSNP: rs11577684
rs11577684
1 1 43788609 intron variant C/G snv 0.27 0.700 1.000 1 2018 2018
dbSNP: rs12410444
rs12410444
2 1.000 0.040 1 43723048 intron variant A/G snv 0.25 0.700 1.000 1 2019 2019
dbSNP: rs246776
rs246776
1 1 43809028 intron variant C/T snv 0.45 0.700 1.000 1 2018 2018
dbSNP: rs2486012
rs2486012
1 1 43907737 intron variant A/G snv 9.3E-02 0.700 1.000 1 2019 2019
dbSNP: rs2906455
rs2906455
1 1 43876223 intron variant T/C snv 0.91 0.700 1.000 1 2018 2018
dbSNP: rs4660261
rs4660261
1 1 43763926 intron variant G/A snv 0.69 0.700 1.000 1 2019 2019
dbSNP: rs4660749
rs4660749
1 1 43784630 intron variant T/G snv 0.90 0.700 1.000 1 2018 2018
dbSNP: rs6429637
rs6429637
1 1 43732860 intron variant A/G snv 0.33 0.700 1.000 1 2019 2019
dbSNP: rs6656457
rs6656457
1 1 43767991 intron variant G/A;C snv 0.700 1.000 1 2018 2018