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: rs1801968
rs1801968
7 0.827 0.040 9 129818622 missense variant C/G;T snv 0.13; 4.0E-06 0.010 1.000 1 2017 2017
dbSNP: rs61999318
rs61999318
2 0.925 0.040 17 68420363 missense variant T/C snv 2.5E-03 2.4E-03 0.010 1.000 1 2015 2015
dbSNP: rs1182
rs1182
9 0.790 0.160 9 129813781 3 prime UTR variant C/A snv 0.17 0.010 1.000 1 2017 2017