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: 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: rs113422242
rs113422242
14 0.763 0.240 15 48510065 stop gained G/A snv 7.0E-06 0.700 0
dbSNP: rs113812345
rs113812345
10 0.790 0.160 15 48513591 stop gained G/A 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: rs1555397413
rs1555397413
13 0.732 0.280 15 48470705 missense variant T/C snv 0.700 0
dbSNP: rs1555398397
rs1555398397
10 0.807 0.240 15 48485436 missense variant C/T snv 0.700 0
dbSNP: rs397515789
rs397515789
10 0.776 0.240 15 48488112 splice donor variant C/A;T snv 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