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: rs121434285
rs121434285
IVD
2 0.925 0.080 15 40411600 missense variant G/T snv 8.0E-06; 8.0E-06 2.1E-05 0.700 1.000 6 1991 2017
dbSNP: rs371427844
rs371427844
IVD
1 1.000 0.080 15 40418165 missense variant C/T snv 4.0E-06 4.2E-05 0.800 1.000 6 1991 2017
dbSNP: rs754600862
rs754600862
IVD
1 1.000 0.080 15 40416336 missense variant T/C snv 8.0E-06 7.0E-06 0.700 1.000 6 1991 2017
dbSNP: rs760822119
rs760822119
IVD
1 1.000 0.080 15 40416293 missense variant T/C snv 4.0E-06 0.700 1.000 6 1991 2017
dbSNP: rs763422682
rs763422682
IVD
1 1.000 0.080 15 40418196 missense variant T/C snv 8.0E-06 0.700 1.000 1 2017 2017