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: rs1554800065
rs1554800065
ANKRD26
2 1.000 0.120 10 27100445 5 prime UTR variant G/C snv 0.700 0
dbSNP: rs863223318
rs863223318
ANKRD26
2 1.000 0.120 10 27100460 5 prime UTR variant C/T snv 0.700 0
dbSNP: rs199683454
rs199683454
ANKRD26
2 0.925 0.160 10 27100324 start lost C/T snv 2.7E-04 2.0E-04 0.010 1.000 1 2017 2017
dbSNP: rs398122374
rs398122374
ITGB3 ; THCAT158
3 0.925 0.120 17 47307567 missense variant T/A;C;G snv 4.0E-06; 4.0E-06 0.010 1.000 1 2013 2013