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 0.800 1.000 5 2010 2019
dbSNP: rs643531
rs643531
TTC39B
2 9 15296036 intron variant C/A snv 0.89 0.800 1.000 2 2010 2018
dbSNP: rs471364
rs471364
TTC39B
3 1.000 0.040 9 15289580 intron variant C/T snv 0.87 0.800 1.000 1 2009 2009
dbSNP: rs540885
rs540885
TTC39B
1 9 15294598 intron variant G/A;C;T snv 0.700 1.000 2 2015 2018
dbSNP: rs686030
rs686030
TTC39B
3 9 15304784 intron variant C/A snv 0.88 0.700 1.000 2 2018 2019
dbSNP: rs1215112
rs1215112
TTC39B
2 9 15303585 intron variant G/A snv 0.89 0.700 1.000 1 2019 2019
dbSNP: rs486349
rs486349
TTC39B
1 9 15293118 intron variant G/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs675849
rs675849
TTC39B
1 9 15298668 intron variant T/A;C;G snv 0.700 1.000 1 2018 2018