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: rs121918399
rs121918399
2 0.925 0.120 19 44907843 missense variant C/T snv 8.0E-06 0.010 1.000 1 2014 2014
dbSNP: rs190853081
rs190853081
3 0.925 0.080 19 44909083 missense variant G/A snv 2.0E-04 5.6E-05 0.010 1.000 1 2014 2014
dbSNP: rs405509
rs405509
30 0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 0.010 1.000 1 2014 2014
dbSNP: rs429358
rs429358
66 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 0.010 1.000 1 2014 2014
dbSNP: rs769446
rs769446
6 0.882 0.120 19 44905371 upstream gene variant T/C snv 7.0E-02 0.010 1.000 1 2014 2014