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: rs137853199
rs137853199
EPHA2
1 1.000 0.040 1 16125304 missense variant C/A snv 0.800 1.000 4 2008 2012
dbSNP: rs137853200
rs137853200
EPHA2
2 0.925 0.120 1 16129440 missense variant G/A snv 0.800 1.000 4 2008 2012
dbSNP: rs886041412
rs886041412
EPHA2
1 1.000 0.040 1 16125329 intron variant C/T snv 0.700 1.000 2 2009 2013
dbSNP: rs116506614
rs116506614
EPHA2
1 1.000 0.040 1 16132227 missense variant C/T snv 7.4E-04 7.1E-04 0.700 0