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: rs28933100
rs28933100
NFKBIA
2 0.925 0.120 14 35404550 missense variant C/A;T snv 0.800 1.000 2 2003 2008
dbSNP: rs121913664
rs121913664
NFKBIA
1 1.000 0.120 14 35404613 stop gained C/T snv 0.700 0
dbSNP: rs121913665
rs121913665
NFKBIA
1 1.000 0.120 14 35404605 stop gained C/A snv 0.700 0
dbSNP: rs1566591073
rs1566591073
NFKBIA
1 1.000 0.120 14 35404535 missense variant A/C;T snv 0.700 0
dbSNP: rs1566591076
rs1566591076
NFKBIA
1 1.000 0.120 14 35404538 missense variant G/T snv 0.700 0
dbSNP: rs1566591082
rs1566591082
NFKBIA
1 1.000 0.120 14 35404549 missense variant G/C snv 0.700 0
dbSNP: rs1566591086
rs1566591086
NFKBIA
1 1.000 0.120 14 35404551 missense variant T/C snv 0.700 0