Source: ALL
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: rs1057518739
rs1057518739
MIPEP
1 1.000 13 23806053 missense variant A/C snv 0.700 0
dbSNP: rs1057518740
rs1057518740
MIPEP
1 1.000 13 23886484 missense variant A/T snv 0.700 0
dbSNP: rs1057518741
rs1057518741
MIPEP
1 1.000 13 23862328 missense variant T/C snv 0.700 0
dbSNP: rs114638163
rs114638163
MIPEP
10 0.827 0.240 13 23805994 stop gained C/A;T snv 4.0E-06; 1.3E-03 0.700 0
dbSNP: rs143912947
rs143912947
MIPEP
1 1.000 13 23869319 missense variant G/A snv 8.1E-06 2.1E-05 0.700 0
dbSNP: rs779598020
rs779598020
MIPEP
1 1.000 13 23837561 missense variant G/C snv 4.4E-05 6.3E-05 0.700 0
dbSNP: rs780533096
rs780533096
MIPEP
44 0.701 0.600 13 23886338 missense variant C/G;T snv 4.8E-06; 9.6E-06 0.700 0