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: rs1156737044
rs1156737044
1 1.000 15 44672106 missense variant A/C snv 6.5E-06 0.800 1.000 0 2017 2017
dbSNP: rs1361024832
rs1361024832
1 1.000 15 44672023 missense variant A/T snv 6.5E-06 0.800 1.000 0 2017 2017
dbSNP: rs1397500378
rs1397500378
1 1.000 15 44669096 missense variant C/T snv 6.6E-06 0.700 1.000 2 2017 2017
dbSNP: rs569729547
rs569729547
1 1.000 15 44669814 missense variant C/T snv 5.2E-05 7.0E-06 0.700 1.000 2 2017 2017
dbSNP: rs1011539285
rs1011539285
1 1.000 15 44669391 missense variant A/G snv 6.5E-06 0.700 0