Gene: TRIM10 ×
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: rs1318638
rs1318638
TRIM10
3 6 30160096 intron variant C/T snv 0.11 0.700 1.000 1 2016 2016
dbSNP: rs144731721
rs144731721
TRIM10
2 6 30157034 missense variant C/T snv 7.3E-03 7.3E-03 0.700 1.000 1 2016 2016