Source: ALL
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: rs886037871
rs886037871
AIP
1 1.000 0.120 11 67483161 start lost G/A snv 0.700 0
dbSNP: rs1287485768
rs1287485768
AIP ; MIR6752
1 1.000 0.120 11 67490081 missense variant C/T snv 0.010 1.000 1 2019 2019
dbSNP: rs267606541
rs267606541
AIP
5 0.827 0.160 11 67487147 stop gained C/T snv 0.010 1.000 1 2012 2012
dbSNP: rs641081
rs641081
AIP ; MIR6752
4 0.851 0.120 11 67490352 missense variant C/A snv 0.96 0.84 0.010 1.000 1 2015 2015
dbSNP: rs745594285
rs745594285
ZNRD2 ; FAM89B ; ZNRD2-AS1
1 1.000 0.120 11 65571531 missense variant A/C snv 4.0E-06 0.010 1.000 1 2012 2012
dbSNP: rs78669402
rs78669402
DCTN6
1 1.000 0.120 8 30179413 missense variant C/A;G snv 6.4E-05; 4.0E-06 0.010 1.000 1 2012 2012