Gene: FAM155A ×
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: rs113226428
rs113226428
FAM155A ; FAM155A-IT1 ; LOC107984581
1 13 107817853 intron variant -/C ins 0.700 1.000 1 2012 2012
dbSNP: rs1539134
rs1539134
FAM155A
1 13 107726915 intron variant G/C;T snv 0.700 1.000 1 2013 2013
dbSNP: rs1557093
rs1557093
FAM155A
1 13 107725887 intron variant C/T snv 0.87 0.700 1.000 1 2013 2013
dbSNP: rs2391566
rs2391566
FAM155A
1 13 107732899 intron variant G/A snv 0.84 0.700 1.000 1 2013 2013
dbSNP: rs371373771
rs371373771
FAM155A ; FAM155A-IT1 ; LOC107984581
1 13 107817853 intron variant G/C snv 0.700 1.000 1 2012 2012
dbSNP: rs3905064
rs3905064
FAM155A
1 13 107730794 intron variant A/G snv 0.74 0.700 1.000 1 2013 2013
dbSNP: rs3915937
rs3915937
FAM155A
1 13 107722352 intron variant C/T snv 0.74 0.700 1.000 1 2013 2013
dbSNP: rs4772910
rs4772910
FAM155A
1 13 107684525 intron variant C/T snv 0.86 0.700 1.000 1 2013 2013
dbSNP: rs7139631
rs7139631
FAM155A
1 13 107691801 intron variant A/G snv 0.12 0.700 1.000 1 2013 2013
dbSNP: rs7319801
rs7319801
FAM155A
1 13 107734296 intron variant G/A snv 0.75 0.700 1.000 1 2013 2013
dbSNP: rs7330529
rs7330529
FAM155A
1 13 107732933 intron variant A/G snv 0.79 0.700 1.000 1 2013 2013
dbSNP: rs9301253
rs9301253
FAM155A
1 13 107725527 intron variant T/C snv 0.71 0.700 1.000 1 2013 2013
dbSNP: rs9520550
rs9520550
FAM155A
1 13 107684706 intron variant A/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs9520568
rs9520568
FAM155A
1 13 107742527 intron variant C/T snv 0.70 0.700 1.000 1 2013 2013
dbSNP: rs9555405
rs9555405
FAM155A
1 13 107733026 intron variant A/C snv 0.74 0.700 1.000 1 2013 2013