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: rs140781106
rs140781106
ITGA3
1 1.000 17 50076642 missense variant G/A;C snv 3.2E-05; 4.0E-06 0.800 0
dbSNP: rs745505565
rs745505565
ITGA3
1 1.000 17 50071380 missense variant G/A snv 8.0E-06 0.700 1.000 2 2012 2016
dbSNP: rs540704248
rs540704248
ITGA3
1 1.000 17 50077024 missense variant C/G;T snv 8.2E-06 0.700 1.000 1 2016 2016
dbSNP: rs797045048
rs797045048
ITGA3
1 1.000 17 50077122 splice donor variant G/A snv 0.700 1.000 1 2016 2016
dbSNP: rs1567701091
rs1567701091
ITGA3
1 1.000 17 50075598 splice acceptor variant G/A snv 0.700 0
dbSNP: rs797044989
rs797044989
ITGA3
1 1.000 17 50074452 missense variant C/T snv 1.2E-05 0.700 0