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: rs137852650
rs137852650
1 1.000 0.080 19 18786040 missense variant C/A snv 0.810 1.000 13 1995 2012
dbSNP: rs137852655
rs137852655
2 0.925 0.080 19 18783125 missense variant C/T snv 0.810 1.000 13 1995 2012
dbSNP: rs137852651
rs137852651
1 1.000 0.080 19 18786051 missense variant C/T snv 0.800 1.000 12 1995 2012
dbSNP: rs137852653
rs137852653
1 1.000 0.080 19 18787644 missense variant A/G snv 0.800 1.000 12 1995 2012
dbSNP: rs137852656
rs137852656
1 1.000 0.080 19 18787584 missense variant A/G snv 0.800 1.000 12 1995 2012
dbSNP: rs312262901
rs312262901
1 1.000 0.080 19 18785050 missense variant T/C snv 0.710 1.000 1 2004 2004
dbSNP: rs1359984033
rs1359984033
1 1.000 0.080 19 18785789 missense variant C/T snv 4.0E-06 0.700 1.000 12 1995 2012
dbSNP: rs557483957
rs557483957
1 1.000 0.080 19 18788654 missense variant G/A snv 2.4E-04 2.4E-04 0.700 1.000 12 1995 2012
dbSNP: rs1555791556
rs1555791556
2 0.925 0.080 19 18787500 missense variant C/A snv 0.700 0
dbSNP: rs193922900
rs193922900
2 0.925 0.080 19 18786035 inframe insertion TCG/-;TCGTCG;TCGTCGTCG delins 0.700 0
dbSNP: rs28936669
rs28936669
1 1.000 0.080 19 18786036 missense variant T/C snv 0.700 0
dbSNP: rs312262899
rs312262899
1 1.000 0.080 19 18785063 missense variant C/G;T snv 0.700 0
dbSNP: rs312262900
rs312262900
1 1.000 0.080 19 18785056 missense variant G/A;C;T snv 0.700 0
dbSNP: rs312262903
rs312262903
1 1.000 0.080 19 18785755 missense variant G/A snv 0.700 0
dbSNP: rs312262904
rs312262904
1 1.000 0.080 19 18783126 missense variant C/T snv 0.700 0
dbSNP: rs142274526
rs142274526
1 1.000 0.080 19 18787572 missense variant G/A;C snv 2.8E-05; 4.0E-06 0.010 1.000 1 2019 2019