Gene: FAM13A ×
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: rs2869967
rs2869967
FAM13A ; LOC105377327
11 0.827 0.120 4 88948181 intron variant T/C snv 0.49 0.800 1.000 2 2012 2015
dbSNP: rs10015415
rs10015415
FAM13A
2 4 89007052 intron variant T/C snv 0.54 0.700 1.000 1 2015 2015
dbSNP: rs10019681
rs10019681
FAM13A
2 4 88911381 intron variant C/T snv 0.28 0.700 1.000 1 2015 2015
dbSNP: rs10021465
rs10021465
FAM13A
4 4 88829210 intron variant A/G snv 0.37 0.700 1.000 1 2015 2015
dbSNP: rs10028589
rs10028589
FAM13A
2 4 88919909 intron variant C/T snv 0.29 0.700 1.000 1 2015 2015
dbSNP: rs12648534
rs12648534
FAM13A
2 4 88878055 intron variant C/T snv 0.29 0.700 1.000 1 2015 2015
dbSNP: rs147089648
rs147089648
FAM13A ; LOC105377327
2 4 88953220 intron variant C/A;T snv 0.700 1.000 1 2015 2015
dbSNP: rs1708667
rs1708667
FAM13A
2 4 89008459 intron variant T/G snv 0.54 0.700 1.000 1 2015 2015
dbSNP: rs1795720
rs1795720
FAM13A
2 4 89008103 intron variant C/T snv 0.54 0.700 1.000 1 2015 2015
dbSNP: rs1795739
rs1795739
FAM13A
2 4 89009162 intron variant A/G snv 0.54 0.700 1.000 1 2015 2015
dbSNP: rs1812329
rs1812329
FAM13A ; LOC105377327
2 4 88948767 intron variant G/A snv 0.47 0.700 1.000 1 2015 2015
dbSNP: rs1964516
rs1964516
FAM13A ; LOC105377327
3 1.000 0.040 4 88954758 intron variant C/T snv 0.45 0.700 1.000 1 2015 2015
dbSNP: rs2013701
rs2013701
FAM13A
5 1.000 0.040 4 88963935 intron variant G/T snv 0.51 0.700 1.000 1 2015 2015
dbSNP: rs2045517
rs2045517
FAM13A ; LOC105377327
5 4 88949813 intron variant C/T snv 0.49 0.700 1.000 1 2015 2015
dbSNP: rs2178586
rs2178586
FAM13A
2 4 89004169 intron variant C/G;T snv 0.54 0.700 1.000 1 2015 2015
dbSNP: rs28455964
rs28455964
FAM13A
2 4 88849758 intron variant T/G snv 0.38 0.700 1.000 1 2015 2015
dbSNP: rs28529050
rs28529050
FAM13A
2 4 88899639 intron variant A/G snv 0.30 0.700 1.000 1 2015 2015
dbSNP: rs2869966
rs2869966
FAM13A ; LOC105377327
9 1.000 0.040 4 88947927 intron variant C/T snv 0.47 0.700 1.000 1 2015 2015
dbSNP: rs2904259
rs2904259
FAM13A
5 4 88964563 intron variant T/A;C snv 0.700 1.000 1 2015 2015
dbSNP: rs4416442
rs4416442
FAM13A ; LOC105377327
4 0.925 0.080 4 88945562 intron variant T/C snv 0.45 0.700 1.000 1 2015 2015
dbSNP: rs4693973
rs4693973
FAM13A
1 4 88876516 intron variant T/A;C snv 0.700 1.000 1 2015 2015
dbSNP: rs4693974
rs4693974
FAM13A
1 4 88889244 intron variant A/G snv 0.56 0.700 1.000 1 2015 2015
dbSNP: rs4693975
rs4693975
FAM13A
2 4 88900733 intron variant C/T snv 0.29 0.700 1.000 1 2015 2015
dbSNP: rs4693976
rs4693976
FAM13A
2 4 88918689 intron variant T/C snv 0.29 0.700 1.000 1 2015 2015
dbSNP: rs4693977
rs4693977
FAM13A ; LOC105377327
2 4 88932928 intron variant T/A snv 0.29 0.700 1.000 1 2015 2015