Gene: MYH9 ×
Source: UNIPROT ×
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: rs80338831
rs80338831
MYH9
1 0.882 0.320 22 36292060 missense variant C/A;G;T snv 0.830 1.000 11 2000 2011
dbSNP: rs80338834
rs80338834
MYH9
1 0.925 0.160 22 36284474 missense variant C/T snv 0.830 1.000 11 2000 2006
dbSNP: rs80338826
rs80338826
MYH9
1 0.827 0.320 22 36305985 missense variant G/A snv 0.810 1.000 11 2000 2006
dbSNP: rs80338827
rs80338827
MYH9
1 0.882 0.320 22 36305984 missense variant C/T snv 7.0E-06 0.810 1.000 11 2000 2006
dbSNP: rs121913655
rs121913655
MYH9
1 1.000 0.160 22 36348958 missense variant G/A;C snv 2.4E-05 0.800 1.000 11 2000 2006
dbSNP: rs121913656
rs121913656
MYH9
1 22 36295526 missense variant G/A snv 0.800 1.000 11 2000 2006
dbSNP: rs121913657
rs121913657
MYH9
1 0.882 0.160 22 36348950 missense variant G/A snv 0.800 1.000 11 2000 2006
dbSNP: rs80338829
rs80338829
MYH9
1 0.851 0.200 22 36295069 missense variant G/A snv 0.800 1.000 11 2000 2006
dbSNP: rs80338830
rs80338830
MYH9
1 0.925 0.160 22 36295068 missense variant C/A snv 0.800 1.000 11 2000 2006
dbSNP: rs200901330
rs200901330
MYH9
1 22 36295650 missense variant A/G snv 3.2E-04 4.3E-04 0.700 1.000 11 2000 2006
dbSNP: rs554332083
rs554332083
MYH9
1 22 36300961 missense variant T/G snv 1.6E-04 2.8E-05 0.700 1.000 11 2000 2006
dbSNP: rs762773112
rs762773112
MYH9
1 22 36285158 missense variant T/C snv 1.6E-05 7.0E-06 0.700 1.000 11 2000 2006
dbSNP: rs76368635
rs76368635
MYH9
1 22 36292132 missense variant G/A snv 1.0E-03 1.2E-03 0.700 1.000 11 2000 2006