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: rs147089648
rs147089648
FAM13A ; LOC105377327
2 4 88953220 intron variant C/A;T snv 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: rs4693973
rs4693973
FAM13A
1 4 88876516 intron variant T/A;C snv 0.700 1.000 1 2015 2015
dbSNP: rs6823536
rs6823536
FAM13A
2 4 89007381 intron variant C/A;T snv 0.700 1.000 1 2015 2015
dbSNP: rs7660385
rs7660385
FAM13A ; LOC105377327
2 4 88939668 intron variant T/C;G snv 0.700 1.000 1 2015 2015
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: rs6835019
rs6835019
FAM13A
2 4 88926504 intron variant A/G snv 0.27 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: rs58281712
rs58281712
FAM13A
2 4 88889805 intron variant G/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
dbSNP: rs12648534
rs12648534
FAM13A
2 4 88878055 intron variant C/T snv 0.29 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: rs7668636
rs7668636
FAM13A
2 4 88898156 intron variant T/C snv 0.29 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: rs62310476
rs62310476
FAM13A
2 4 88911177 intron variant T/A 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: rs7695732
rs7695732
FAM13A
2 4 88911640 intron variant G/C snv 0.29 0.700 1.000 1 2015 2015
dbSNP: rs62308746
rs62308746
FAM13A
2 4 88884818 intron variant T/C snv 0.29 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: rs7687539
rs7687539
FAM13A
2 4 88885633 intron variant G/A snv 0.30 0.700 1.000 1 2015 2015
dbSNP: rs62308745
rs62308745
FAM13A
2 4 88880152 intron variant T/C snv 0.30 0.700 1.000 1 2015 2015
dbSNP: rs7682431
rs7682431
FAM13A
2 4 88844510 intron variant G/C snv 0.36 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: rs6830970
rs6830970
FAM13A
5 1.000 0.040 4 88855930 3 prime UTR variant A/G snv 0.38 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