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: rs587776991
rs587776991
PIEZO1
1 1.000 0.200 16 88719665 missense variant G/A snv 3.7E-05 3.5E-05 0.800 1.000 2 2013 2013
dbSNP: rs587776987
rs587776987
PIEZO1 ; MIR4722
1 1.000 0.200 16 88716885 missense variant A/C snv 0.800 0
dbSNP: rs587776988
rs587776988
PIEZO1 ; CTU2 ; MIR4722
1 1.000 0.200 16 88715804 missense variant C/T snv 0.800 0
dbSNP: rs587776989
rs587776989
PIEZO1
1 1.000 0.200 16 88720175 missense variant C/T snv 0.800 0
dbSNP: rs587776990
rs587776990
PIEZO1
1 1.000 0.200 16 88725505 missense variant C/G snv 0.800 0
dbSNP: rs200970763
rs200970763
PIEZO1 ; LOC100289580
1 1.000 0.200 16 88733731 missense variant C/A;T snv 3.8E-03 0.700 1.000 6 2012 2014
dbSNP: rs587777764
rs587777764
PIEZO1
1 1.000 0.200 16 88720174 missense variant G/A snv 0.700 1.000 6 2012 2014
dbSNP: rs587777765
rs587777765
PIEZO1
1 1.000 0.200 16 88727144 missense variant G/A snv 1.3E-05 0.700 1.000 6 2012 2014
dbSNP: rs202103485
rs202103485
PIEZO1 ; LOC100289580
1 1.000 0.200 16 88733652 missense variant C/A;T snv 3.8E-03 4.1E-03 0.700 0
dbSNP: rs587776992
rs587776992
PIEZO1 ; CTU2
1 1.000 0.200 16 88715683 inframe insertion AGCTCC/-;AGCTCCAGCTCC delins 0.700 0
dbSNP: rs749288233
rs749288233
PIEZO1 ; CTU2
2 0.925 0.200 16 88715708 missense variant C/T snv 6.4E-06 0.700 0
dbSNP: rs755885744
rs755885744
PIEZO1 ; LOC100289580
1 1.000 0.200 16 88734384 missense variant C/T snv 4.0E-05 2.8E-05 0.700 0