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: rs1057518909
rs1057518909
5 0.925 0.120 15 48534099 frameshift variant CATT/- delins 0.700 0
dbSNP: rs1085308004
rs1085308004
9 0.807 0.240 15 48425420 missense variant A/G snv 0.700 0
dbSNP: rs112550005
rs112550005
18 0.742 0.240 15 48425829 stop gained G/A snv 0.700 0
dbSNP: rs113812345
rs113812345
10 0.790 0.160 15 48513591 stop gained G/A snv 0.700 0
dbSNP: rs1232880706
rs1232880706
36 0.689 0.440 15 48526247 stop gained C/A;T snv 0.700 0
dbSNP: rs137854461
rs137854461
12 0.790 0.280 15 48437026 missense variant T/C snv 0.700 0
dbSNP: rs137854466
rs137854466
23 0.724 0.320 15 48411280 stop gained G/A;C snv 4.0E-05; 8.0E-06 0.700 0
dbSNP: rs1555398397
rs1555398397
10 0.807 0.240 15 48485436 missense variant C/T snv 0.700 0
dbSNP: rs1555398673
rs1555398673
7 0.807 0.200 15 48488433 missense variant A/G snv 0.700 0
dbSNP: rs727503054
rs727503054
15 0.732 0.200 15 48420752 missense variant A/G;T snv 1.6E-05 0.700 0
dbSNP: rs761857514
rs761857514
8 0.851 0.240 15 48452676 stop gained C/A;T snv 4.0E-06 0.700 0