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: rs10010325
rs10010325
4 1.000 0.040 4 105185196 intron variant C/A;G;T snv 0.700 1.000 2 2018 2019
dbSNP: rs11726786
rs11726786
1 4 105199599 intron variant T/A;G snv 0.700 1.000 2 2017 2019
dbSNP: rs1391438
rs1391438
1 4 105230686 intron variant T/C snv 0.71 0.700 1.000 2 2018 2018
dbSNP: rs2647249
rs2647249
1 4 105264506 intron variant C/T snv 0.82 0.700 1.000 2 2018 2018
dbSNP: rs1391440
rs1391440
1 4 105195804 intron variant C/G snv 0.50 0.700 1.000 1 2019 2019
dbSNP: rs2454205
rs2454205
1 4 105263072 intron variant C/T snv 0.43 0.700 1.000 1 2018 2018
dbSNP: rs2647257
rs2647257
1 4 105278348 3 prime UTR variant A/T snv 0.27 0.700 1.000 1 2019 2019
dbSNP: rs2903385
rs2903385
2 4 105173270 intron variant G/A snv 0.49 0.700 1.000 1 2018 2018
dbSNP: rs6839705
rs6839705
1 4 105223578 intron variant A/C snv 0.61 0.700 1.000 1 2019 2019
dbSNP: rs7674220
rs7674220
2 1.000 0.040 4 105227601 intron variant G/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs7683416
rs7683416
2 4 105231827 intron variant T/C snv 0.45 0.700 1.000 1 2018 2018