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: rs1260326
rs1260326
GCKR
81 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 0.700 1.000 1 2013 2013
dbSNP: rs3135002
rs3135002 		2 1.000 0.120 6 32700662 TF binding site variant A/C snv 0.80 0.700 1.000 1 2018 2018
dbSNP: rs4841132
rs4841132
LOC157273
14 8 9326086 non coding transcript exon variant A/G snv 0.89 0.700 1.000 1 2013 2013
dbSNP: rs559047
rs559047 		2 1.000 0.120 1 238590616 intergenic variant T/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs61211515
rs61211515 		2 1.000 0.120 6 30133199 upstream gene variant TT/-;T;TTT;TTTT delins 0.14 0.700 1.000 1 2018 2018
dbSNP: rs6517656
rs6517656
BACE2
1 21 41211811 intron variant G/A snv 0.34 0.700 1.000 1 2013 2013
dbSNP: rs9260151
rs9260151
HLA-A
2 1.000 0.120 6 29943253 non coding transcript exon variant C/T snv 0.16 0.14 0.700 1.000 1 2018 2018