Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs73071352
rs73071352
0.882 0.160 3 41786808 intron variant A/G snv 0.12
Monoclonal Gammopathy of Undetermined Significance
Immune System Diseases; Hemic and Lymphatic Diseases 0.700 1.000 1 2015 2015
dbSNP: rs9848754
rs9848754
0.882 0.160 3 41712155 intron variant C/T snv 0.18
Monoclonal Gammopathy of Undetermined Significance
Immune System Diseases; Hemic and Lymphatic Diseases 0.700 1.000 1 2019 2019
dbSNP: rs1052501
rs1052501
0.925 0.160 3 41883906 missense variant C/G;T snv 0.80
Monoclonal Gammopathy of Undetermined Significance
Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2014 2014