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: rs75002628
rs75002628
ALB
2 0.925 0.080 4 73412007 missense variant G/A;C snv 7.2E-05 0.820 1.000 6 1994 2019
dbSNP: rs77892378
rs77892378
ALB
1 1.000 0.080 4 73406760 missense variant T/C;G snv 0.800 1.000 4 1994 1998
dbSNP: rs1444083785
rs1444083785
TXNRD2
1 1.000 0.080 22 19895544 missense variant T/C snv 7.0E-06 0.010 1.000 1 2018 2018
dbSNP: rs1481789776
rs1481789776
TXNRD2
1 1.000 0.080 22 19883384 missense variant C/T snv 4.0E-06 7.0E-06 0.010 1.000 1 2018 2018