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: rs121434427
rs121434427
NDUFS2
1 1.000 1 161209912 missense variant G/A snv 0.800 1.000 1 2001 2001
dbSNP: rs121434428
rs121434428
NDUFS2
1 1.000 1 161209915 missense variant C/A snv 0.800 1.000 1 2001 2001
dbSNP: rs121434429
rs121434429
FCER1G ; NDUFS2
1 1.000 1 161213673 missense variant T/C snv 7.0E-06 0.800 1.000 1 2001 2001