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: rs730880014
rs730880014
MAFB
1 1.000 0.040 20 40688690 missense variant G/A snv 0.810 1.000 1 2017 2017
dbSNP: rs387907004
rs387907004
MAFB
1 1.000 0.040 20 40688667 missense variant T/G snv 0.800 1.000 1 2012 2012
dbSNP: rs387907005
rs387907005
MAFB
1 1.000 0.040 20 40688643 missense variant A/C snv 0.800 1.000 1 2012 2012
dbSNP: rs387907006
rs387907006
MAFB
1 1.000 0.040 20 40688642 missense variant G/A snv 0.800 1.000 1 2012 2012
dbSNP: rs387907007
rs387907007
MAFB
1 1.000 0.040 20 40688640 missense variant G/A snv 0.800 1.000 1 2012 2012
dbSNP: rs387907008
rs387907008
MAFB
1 1.000 0.040 20 40688639 missense variant G/A snv 0.800 1.000 1 2012 2012
dbSNP: rs1555826433
rs1555826433
MAFB
1 1.000 0.040 20 40688645 missense variant G/A snv 0.700 1.000 1 2012 2012