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: rs6265
rs6265
272 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 0.100 0.833 30 2002 2020
dbSNP: rs759834365
rs759834365
237 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 0.100 0.821 28 2002 2019
dbSNP: rs746682028
rs746682028
36 0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 0.100 0.700 10 2004 2019
dbSNP: rs764254110
rs764254110
1 1.000 0.040 11 27658495 missense variant C/T snv 2.8E-05 1.4E-05 0.030 1.000 3 2016 2019
dbSNP: rs370102323
rs370102323
2 0.925 0.080 11 27658085 synonymous variant C/A;T snv 4.0E-06; 4.4E-05 0.010 1.000 1 2005 2005
dbSNP: rs893924483
rs893924483
23 0.716 0.280 11 27658285 missense variant C/A;T snv 4.0E-06 1.4E-05 0.010 1.000 1 2018 2018