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: rs397514698
rs397514698
52 0.667 0.400 9 77797577 missense variant C/T snv 0.020 1.000 2 2014 2016
dbSNP: rs797044883
rs797044883
4 0.882 0.160 15 23645831 stop gained G/A snv 0.700 0
dbSNP: rs1179275735
rs1179275735
MYB
1 1.000 0.120 6 135192344 missense variant A/G snv 0.010 1.000 1 2014 2014
dbSNP: rs756463754
rs756463754
1 1.000 0.120 6 135201724 missense variant A/G snv 0.010 1.000 1 2014 2014
dbSNP: rs775607970
rs775607970
1 1.000 0.120 6 135197028 missense variant A/C;G snv 4.0E-06; 4.0E-06 0.010 1.000 1 2014 2014
dbSNP: rs1338652552
rs1338652552
1 1.000 0.120 5 150133900 stop gained C/T snv 0.010 1.000 1 2014 2014
dbSNP: rs1442264858
rs1442264858
2 0.925 0.160 5 150132750 missense variant C/T snv 4.1E-06 0.010 1.000 1 2014 2014
dbSNP: rs767439253
rs767439253
1 1.000 0.120 3 179199885 missense variant A/G snv 1.1E-04 1.4E-05 0.010 1.000 1 2014 2014