Gene: AP1G1 ×
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: rs10459804
rs10459804
AP1G1
1 16 71799928 intron variant A/T snv 0.33 0.700 1.000 1 2012 2012
dbSNP: rs11075900
rs11075900
AP1G1
1 16 71749470 intron variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs11075902
rs11075902
AP1G1
1 16 71775185 intron variant C/T snv 0.33 0.700 1.000 1 2012 2012
dbSNP: rs11539980
rs11539980
AP1G1
1 16 71731513 3 prime UTR variant G/C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs11641873
rs11641873
AP1G1
1 16 71740993 intron variant T/G snv 0.39 0.700 1.000 1 2012 2012
dbSNP: rs11645467
rs11645467
AP1G1
1 16 71740487 intron variant G/A snv 0.34 0.700 1.000 1 2012 2012
dbSNP: rs11646635
rs11646635
AP1G1
1 16 71740794 intron variant G/C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs11646748
rs11646748
AP1G1
1 16 71741177 intron variant C/T snv 0.34 0.700 1.000 1 2012 2012
dbSNP: rs11859903
rs11859903
AP1G1
1 16 71747199 5 prime UTR variant C/T snv 8.5E-02 0.700 1.000 1 2012 2012
dbSNP: rs11861285
rs11861285
AP1G1
1 16 71793889 intron variant T/C snv 8.9E-02 0.700 1.000 1 2012 2012
dbSNP: rs11866559
rs11866559
AP1G1 ; SNORD71
1 16 71758287 intron variant G/A snv 0.23 0.700 1.000 1 2012 2012
dbSNP: rs12447856
rs12447856
AP1G1
1 16 71756770 intron variant C/T snv 0.33 0.700 1.000 1 2012 2012
dbSNP: rs12920243
rs12920243
AP1G1
1 16 71767691 intron variant G/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs12930206
rs12930206
AP1G1
1 16 71766481 intron variant T/A snv 0.39 0.28 0.700 1.000 1 2012 2012
dbSNP: rs1392483
rs1392483
AP1G1
1 16 71788328 intron variant C/T snv 0.34 0.700 1.000 1 2012 2012
dbSNP: rs2036338
rs2036338
AP1G1
1 16 71754927 intron variant G/C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs2270830
rs2270830
AP1G1
1 16 71748541 intron variant A/G snv 0.34 0.700 1.000 1 2012 2012
dbSNP: rs2270831
rs2270831
AP1G1
1 16 71746696 splice region variant T/C snv 0.40 0.34 0.700 1.000 1 2012 2012
dbSNP: rs2270832
rs2270832
AP1G1
1 16 71746582 splice region variant G/A;T snv 0.40 0.700 1.000 1 2012 2012
dbSNP: rs2278031
rs2278031
AP1G1
1 16 71734597 non coding transcript exon variant T/A;C snv 2.0E-05; 0.40 0.700 1.000 1 2012 2012
dbSNP: rs28704189
rs28704189
AP1G1
1 16 71792095 intron variant G/A snv 0.34 0.700 1.000 1 2012 2012
dbSNP: rs35173463
rs35173463
AP1G1
1 16 71744737 intron variant G/A snv 0.34 0.700 1.000 1 2012 2012
dbSNP: rs3751817
rs3751817
AP1G1
1 16 71730931 3 prime UTR variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs3848389
rs3848389
AP1G1
1 16 71806012 intron variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs4788442
rs4788442
AP1G1
1 16 71743545 non coding transcript exon variant G/C snv 0.34 0.700 1.000 1 2012 2012