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: rs137853112
rs137853112
KLHL7
2 0.925 0.080 7 23140775 missense variant G/A snv 0.800 1.000 4 2009 2011
dbSNP: rs137853113
rs137853113
KLHL7
2 0.925 0.080 7 23140784 missense variant C/T snv 0.800 1.000 4 2009 2011
dbSNP: rs137853114
rs137853114
KLHL7
2 0.925 0.080 7 23140783 missense variant G/A snv 0.800 1.000 4 2009 2011