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: rs879255247
rs879255247
1 1.000 0.200 19 5694889 missense variant G/A snv 4.0E-06 0.800 1.000 2 2015 2015
dbSNP: rs879255248
rs879255248
1 1.000 0.200 19 5696253 missense variant G/T snv 0.800 1.000 2 2015 2015
dbSNP: rs879255249
rs879255249
1 1.000 0.200 19 5694536 missense variant G/A snv 0.800 1.000 2 2015 2015
dbSNP: rs549574673
rs549574673
1 1.000 0.200 19 5694879 missense variant C/T snv 4.4E-05 2.1E-05 0.700 1.000 2 2015 2015
dbSNP: rs770036526
rs770036526
1 1.000 0.200 19 5696058 missense variant G/A snv 8.1E-06 0.700 1.000 2 2015 2015
dbSNP: rs777009012
rs777009012
1 1.000 0.200 19 5694901 missense variant G/A snv 4.8E-05 5.6E-05 0.700 1.000 2 2015 2015
dbSNP: rs147588238
rs147588238
1 1.000 0.200 19 5694546 missense variant G/A;C snv 8.0E-06; 8.0E-06 0.700 0
dbSNP: rs562553348
rs562553348
1 1.000 0.200 19 5694407 missense variant C/T snv 0.700 0
dbSNP: rs730880293
rs730880293
1 1.000 0.200 19 5693737 missense variant T/C snv 0.700 0
dbSNP: rs758265405
rs758265405
3 0.882 0.280 19 5692127 missense variant C/T snv 1.6E-05 0.010 < 0.001 1 2018 2018
dbSNP: rs758802403
rs758802403
3 0.882 0.280 19 5694510 missense variant C/T snv 2.0E-05 2.1E-05 0.010 < 0.001 1 2018 2018
dbSNP: rs764931850
rs764931850
3 0.882 0.280 19 5696750 missense variant A/G snv 0.010 < 0.001 1 2018 2018