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: rs137853197
rs137853197
NEXN
3 0.925 0.040 1 77942756 missense variant A/G snv 7.2E-05 1.0E-04 0.800 1.000 1 2009 2009
dbSNP: rs137853198
rs137853198
NEXN
1 1.000 0.040 1 77942632 missense variant C/A snv 0.800 1.000 1 2009 2009
dbSNP: rs771262904
rs771262904
NEXN
1 1.000 0.040 1 77926827 stop gained G/T snv 4.0E-06 7.0E-06 0.700 0