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: rs886037734
rs886037734
1 1.000 19 17341599 missense variant G/A snv 0.800 1.000 2 2014 2016
dbSNP: rs886037735
rs886037735
1 1.000 19 17341078 missense variant G/C snv 0.800 1.000 2 2014 2016
dbSNP: rs730880255
rs730880255
1 1.000 19 17338626 missense variant A/T snv 0.800 0
dbSNP: rs373370177
rs373370177
1 1.000 19 17339123 missense variant C/A;G snv 4.0E-06; 2.0E-05 0.700 1.000 2 2014 2016
dbSNP: rs1057518138
rs1057518138
1 1.000 19 17337619 missense variant G/C;T snv 0.700 0
dbSNP: rs1274363168
rs1274363168
1 1.000 19 17338667 missense variant C/T snv 4.0E-06 0.700 0
dbSNP: rs1555726849
rs1555726849
1 1.000 19 17339005 stop gained G/T snv 0.700 0
dbSNP: rs372174278
rs372174278
1 1.000 19 17339589 missense variant G/C;T snv 1.2E-04; 4.3E-06 0.700 0
dbSNP: rs770871640
rs770871640
1 1.000 19 17341181 missense variant T/C snv 4.0E-06 0.700 0
dbSNP: rs774708853
rs774708853
1 1.000 19 17338590 missense variant C/T snv 8.0E-06 0.700 0
dbSNP: rs869320746
rs869320746
1 1.000 19 17341512 frameshift variant -/C delins 0.700 0
dbSNP: rs886037736
rs886037736
1 1.000 19 17337643 frameshift variant AA/GTG delins 0.700 0