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: rs397514510
rs397514510
INPPL1
1 1.000 0.080 11 72233098 missense variant C/T snv 0.800 1.000 1 2013 2013
dbSNP: rs397514511
rs397514511
INPPL1
1 1.000 0.080 11 72230799 missense variant C/T snv 0.800 1.000 1 2013 2013
dbSNP: rs397514512
rs397514512
INPPL1
1 1.000 0.080 11 72233696 stop gained T/A snv 0.800 1.000 1 2013 2013
dbSNP: rs397514508
rs397514508
INPPL1
1 1.000 0.080 11 72233099 missense variant C/T snv 0.700 1.000 1 2013 2013
dbSNP: rs397514509
rs397514509
INPPL1
1 1.000 0.080 11 72229116 stop gained C/A;G;T snv 4.0E-06; 1.2E-05 0.700 1.000 1 2013 2013
dbSNP: rs746647683
rs746647683
INPPL1
1 1.000 0.080 11 72229677 frameshift variant AG/- del 1.4E-05 0.700 1.000 1 2013 2013
dbSNP: rs878853123
rs878853123
INPPL1
1 1.000 0.080 11 72233471 missense variant C/T snv 0.700 1.000 1 2013 2013
dbSNP: rs1135401750
rs1135401750
INPPL1
1 1.000 0.080 11 72232757 frameshift variant -/T delins 0.700 0
dbSNP: rs655423
rs655423
INPPL1
1 1.000 0.080 11 72234616 splice donor variant G/A;C snv 0.700 0
dbSNP: rs797044468
rs797044468
INPPL1
1 1.000 0.080 11 72229677 frameshift variant A/- del 0.700 0
dbSNP: rs797044469
rs797044469
INPPL1
1 1.000 0.080 11 72228377 frameshift variant AGACC/- delins 0.700 0
dbSNP: rs797044470
rs797044470
INPPL1
1 1.000 0.080 11 72225071 frameshift variant GAGGAGCTGCTGGCCCGGGCGGGCCGCG/- delins 0.700 0