Gene: TTC39B ×
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: rs581080
rs581080
TTC39B
3 9 15305380 intron variant G/C snv 0.72 0.700 1.000 2 2010 2013
dbSNP: rs471364
rs471364
TTC39B
3 1.000 0.040 9 15289580 intron variant C/T snv 0.87 0.700 1.000 1 2009 2009
dbSNP: rs643531
rs643531
TTC39B
2 9 15296036 intron variant C/A snv 0.89 0.700 1.000 1 2010 2010