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: rs121918464
rs121918464
PTPN11
25 0.708 0.440 12 112450406 missense variant G/A;C snv 0.010 1.000 1 2018 2018
dbSNP: rs371663652
rs371663652
FLT3
1 1.000 0.040 13 28062006 missense variant C/T snv 4.0E-05 6.3E-05 0.010 1.000 1 2018 2018
dbSNP: rs587782006
rs587782006
TP53
2 0.925 0.040 17 7673761 missense variant C/T snv 4.0E-06 0.010 1.000 1 2018 2018
dbSNP: rs750949764
rs750949764
FOS
2 1.000 0.040 14 75280958 missense variant G/C snv 4.0E-06 0.010 1.000 1 2018 2018