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: rs10062446
rs10062446
KIF3A
1 5 132704682 intron variant T/A snv 0.59 0.010 1.000 1 2008 2008
dbSNP: rs11740584
rs11740584
KIF3A
1 5 132711097 intron variant G/A;C;T snv 4.0E-06; 0.60; 4.0E-06 0.010 1.000 1 2008 2008
dbSNP: rs2070874
rs2070874
IL4
27 0.672 0.560 5 132674018 5 prime UTR variant C/T snv 0.28 0.28 0.010 1.000 1 2008 2008
dbSNP: rs2729835
rs2729835
RPS27L ; LACTB
1 15 63141567 missense variant G/A snv 0.68 0.65 0.010 1.000 1 2008 2008