Gene: FAM13A ×
Source: BEFREE ×
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
2 0.925 0.040 4 88962828 intron variant C/T snv 0.53 0.840 1.000 4 2010 2015
dbSNP: rs2869967
rs2869967
FAM13A ; LOC105377327
4 0.827 0.120 4 88948181 intron variant T/C snv 0.49 0.820 0.750 2 2010 2015
dbSNP: rs1903003
rs1903003
FAM13A
1 0.925 0.080 4 88965146 intron variant C/G;T snv 0.710 1.000 1 2010 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
1 1.000 0.040 4 88963935 intron variant G/T snv 0.51 0.010 1.000 1 2019 2019
dbSNP: rs6830970
rs6830970
FAM13A
1 1.000 0.040 4 88855930 3 prime UTR variant A/G snv 0.38 0.010 1.000 1 2013 2013