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: rs876661297
rs876661297
TRNT1
1 1.000 3 3129166 inframe deletion AAG/- delins 0.700 0
dbSNP: rs876661298
rs876661298
TRNT1 ; CRBN
2 0.925 3 3148095 frameshift variant A/-;AA delins 0.700 0
dbSNP: rs876661299
rs876661299
TRNT1 ; CRBN
1 1.000 3 3146404 intron variant T/C snv 8.5E-06 0.700 0