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: rs111584802
rs111584802
1 1.000 0.080 5 75587055 missense variant A/G snv 0.700 0
dbSNP: rs1304454699
rs1304454699
1 1.000 0.080 5 75590429 missense variant G/A snv 4.0E-06 0.700 0
dbSNP: rs139591993
rs139591993
1 1.000 0.080 5 75596275 missense variant A/C;T snv 4.0E-06 0.700 0
dbSNP: rs148960463
rs148960463
1 1.000 0.080 5 75547107 missense variant G/A snv 2.1E-03 1.4E-03 0.700 0
dbSNP: rs1554059550
rs1554059550
1 1.000 0.080 5 75573793 missense variant T/C snv 0.700 0
dbSNP: rs1554059573
rs1554059573
1 1.000 0.080 5 75573841 missense variant T/C snv 0.700 0
dbSNP: rs1554062741
rs1554062741
1 1.000 0.080 5 75590373 missense variant A/G snv 0.700 0
dbSNP: rs1554062789
rs1554062789
1 1.000 0.080 5 75590408 missense variant C/T snv 0.700 0
dbSNP: rs1554062804
rs1554062804
1 1.000 0.080 5 75590425 synonymous variant G/A snv 0.700 0
dbSNP: rs1554063600
rs1554063600
1 1.000 0.080 5 75593902 stop lost A/G snv 0.700 0
dbSNP: rs1554063656
rs1554063656
1 1.000 0.080 5 75593981 missense variant T/C snv 0.700 0
dbSNP: rs1554064175
rs1554064175
1 1.000 0.080 5 75596345 missense variant A/T snv 0.700 0
dbSNP: rs1554064740
rs1554064740
1 1.000 0.080 5 75598003 missense variant T/G snv 0.700 0
dbSNP: rs749804502
rs749804502
1 1.000 0.080 5 75573790 missense variant G/A;T snv 1.2E-05 2.1E-05 0.700 0
dbSNP: rs770984846
rs770984846
1 1.000 0.080 5 75590368 synonymous variant G/A snv 2.4E-05 1.4E-05 0.700 0
dbSNP: rs781194178
rs781194178
1 1.000 0.080 5 75596385 missense variant G/A;T snv 8.0E-06 0.700 0
dbSNP: rs786205688
rs786205688
1 1.000 0.080 5 75598084 3 prime UTR variant T/C snv 0.700 0
dbSNP: rs863225454
rs863225454
1 1.000 0.080 5 75573739 missense variant C/T snv 0.700 0
dbSNP: rs863225455
rs863225455
1 1.000 0.080 5 75596726 missense variant C/T snv 0.700 0
dbSNP: rs863225456
rs863225456
1 1.000 0.080 5 75596885 missense variant T/A snv 0.700 0
dbSNP: rs863225457
rs863225457
1 1.000 0.080 5 75596434 missense variant G/A snv 0.700 0