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: rs6551665
rs6551665
4 0.882 0.040 4 61873823 intron variant G/A snv 0.59 0.030 1.000 3 2015 2019
dbSNP: rs10001410
rs10001410
1 1.000 0.040 4 61608511 intron variant C/A snv 0.55 0.010 1.000 1 2019 2019
dbSNP: rs1355368
rs1355368
1 1.000 0.040 4 61914104 intron variant A/G;T snv 0.010 1.000 1 2015 2015
dbSNP: rs1565902
rs1565902
1 1.000 0.040 4 61542902 intron variant T/C snv 0.53 0.010 1.000 1 2019 2019
dbSNP: rs1868790
rs1868790
1 1.000 0.040 4 61828999 intron variant T/A;G snv 0.010 1.000 1 2019 2019
dbSNP: rs2122642
rs2122642
1 1.000 0.040 4 61832546 intron variant G/A snv 0.33 0.010 1.000 1 2019 2019
dbSNP: rs6813183
rs6813183
1 1.000 0.040 4 61903413 intron variant G/C snv 0.67 0.010 1.000 1 2015 2015
dbSNP: rs734644
rs734644
1 1.000 0.040 4 61935010 missense variant T/A;C snv 0.69 0.010 1.000 1 2015 2015