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: rs111033570
rs111033570
TRIM32 ; ASTN2
4 0.925 0.160 9 116699201 missense variant G/A snv 8.0E-06 0.820 1.000 5 2002 2011
dbSNP: rs121434447
rs121434447
TRIM32 ; ASTN2
1 1.000 0.120 9 116698923 missense variant G/A snv 3.6E-05 2.1E-05 0.700 1.000 2 2002 2008