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: rs778210210
rs778210210
SLC39A8
1 1.000 4 102344551 missense variant C/G snv 3.2E-05 2.1E-05 0.800 1.000 2 2015 2015
dbSNP: rs373562040
rs373562040
SLC39A8
2 1.000 4 102344566 missense variant C/A;T snv 6.4E-04 0.700 1.000 2 2015 2015
dbSNP: rs864309659
rs864309659
SLC39A8
1 1.000 4 102267901 missense variant A/T snv 0.700 1.000 2 2015 2015
dbSNP: rs864309660
rs864309660
SLC39A8
2 1.000 4 102267916 missense variant C/G snv 0.700 1.000 2 2015 2015
dbSNP: rs779241085
rs779241085
SLC39A8
2 1.000 4 102305054 missense variant C/A snv 6.4E-05 4.9E-05 0.700 0