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: rs6015450
rs6015450
7 20 59176062 intron variant A/G snv 0.14 0.700 1.000 4 2011 2018
dbSNP: rs16982520
rs16982520
4 1.000 0.040 20 59183665 intron variant A/G snv 0.14 0.700 1.000 1 2016 2016
dbSNP: rs259983
rs259983
2 20 59160402 5 prime UTR variant A/C snv 0.25 0.700 1.000 1 2018 2018
dbSNP: rs6026739
rs6026739
1 20 59164414 intron variant A/T snv 0.15 0.700 1.000 1 2019 2019
dbSNP: rs6026748
rs6026748
3 20 59170760 intron variant G/A snv 0.14 0.700 1.000 1 2016 2016
dbSNP: rs73306860
rs73306860
1 20 59150608 intron variant G/A snv 0.13 0.700 1.000 1 2019 2019
dbSNP: rs73306896
rs73306896
2 20 59175478 intron variant C/T snv 0.14 0.700 1.000 1 2018 2018