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: rs121913272
rs121913272
13 0.752 0.400 3 179210192 missense variant T/C;G snv 0.700 0
dbSNP: rs121913275
rs121913275
26 0.672 0.320 3 179218305 missense variant G/A;C;T snv 4.0E-06 0.700 0
dbSNP: rs121913279
rs121913279
101 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 0.700 0
dbSNP: rs121913283
rs121913283
16 0.724 0.440 3 179234286 missense variant G/A;T snv 4.0E-06 0.700 0
dbSNP: rs121913286
rs121913286
23 0.677 0.280 3 179218306 missense variant C/A;G snv 0.700 0
dbSNP: rs1560137609
rs1560137609
2 0.925 0.080 3 179199743 frameshift variant -/T delins 0.700 0
dbSNP: rs397514565
rs397514565
3 0.882 0.240 3 179204576 missense variant G/A snv 0.700 0
dbSNP: rs863225060
rs863225060
2 0.925 0.120 3 179199136 missense variant C/T snv 0.700 0
dbSNP: rs121434592
rs121434592
54 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 0.010 1.000 1 2019 2019