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: rs104895105
rs104895105
MEFV
7 0.851 0.120 16 3247171 missense variant G/A snv 0.010 1.000 1 2004 2004
dbSNP: rs1128501
rs1128501
ABCB1
1 7 87566218 missense variant C/A snv 0.700 0
dbSNP: rs1045642
rs1045642
ABCB1
214 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.010 1.000 1 2011 2011