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: rs7671167
rs7671167
FAM13A
7 0.925 0.040 4 88962828 intron variant C/T snv 0.53 0.840 1.000 6 2010 2015
dbSNP: rs2869967
rs2869967
FAM13A ; LOC105377327
11 0.827 0.120 4 88948181 intron variant T/C snv 0.49 0.820 0.750 4 2010 2015
dbSNP: rs1964516
rs1964516
FAM13A ; LOC105377327
3 1.000 0.040 4 88954758 intron variant C/T snv 0.45 0.800 1.000 1 2012 2012
dbSNP: rs1903003
rs1903003
FAM13A
4 0.925 0.080 4 88965146 intron variant C/G;T snv 0.710 1.000 3 2010 2015
dbSNP: rs2869966
rs2869966
FAM13A ; LOC105377327
9 1.000 0.040 4 88947927 intron variant C/T snv 0.47 0.700 1.000 2 2014 2019
dbSNP: rs4416442
rs4416442
FAM13A ; LOC105377327
4 0.925 0.080 4 88945562 intron variant T/C snv 0.45 0.700 1.000 2 2014 2014
dbSNP: rs6837671
rs6837671
FAM13A ; LOC105377327
4 0.925 0.040 4 88951941 intron variant A/G snv 0.47 0.700 1.000 1 2017 2017
dbSNP: rs7671261
rs7671261
FAM13A
2 1.000 0.040 4 88962667 intron variant G/A snv 0.59 0.700 1.000 1 2019 2019
dbSNP: rs7674369
rs7674369
FAM13A ; LOC105377327
3 1.000 0.040 4 88951025 intron variant G/A;T snv 0.700 1.000 1 2015 2015
dbSNP: rs17014601
rs17014601
FAM13A
1 1.000 0.040 4 88809748 intron variant T/C snv 6.7E-02 0.010 1.000 1 2018 2018
dbSNP: rs2013701
rs2013701
FAM13A
5 1.000 0.040 4 88963935 intron variant G/T snv 0.51 0.010 1.000 1 2019 2019
dbSNP: rs6830970
rs6830970
FAM13A
5 1.000 0.040 4 88855930 3 prime UTR variant A/G snv 0.38 0.010 1.000 1 2013 2013