Gene: AP4B1-AS1 ×
Source: GWASDB ×
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: rs2476601
rs2476601
PTPN22 ; AP4B1-AS1
13 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 1.000 0.877 8 2005 2019
dbSNP: rs12566340
rs12566340
BCL2L15 ; AP4B1-AS1
1 0.925 0.200 1 113877706 3 prime UTR variant C/A;T snv 0.710 0.500 1 2009 2010
dbSNP: rs6665194
rs6665194
AP4B1-AS1
1 1.000 0.120 1 113875221 intron variant G/A;T snv 0.710 1.000 1 2009 2017
dbSNP: rs1217407
rs1217407
PTPN22 ; AP4B1-AS1
1 1.000 0.120 1 113851126 intron variant A/G snv 0.77 0.700 1.000 1 2009 2009
dbSNP: rs1217413
rs1217413
PTPN22 ; AP4B1-AS1
1 1.000 0.120 1 113815128 intron variant G/A snv 0.82 0.700 1.000 1 2007 2007
dbSNP: rs1217418
rs1217418
PTPN22 ; AP4B1-AS1
1 0.925 0.120 1 113858609 intron variant A/G snv 0.53 0.57 0.700 1.000 1 2009 2009
dbSNP: rs7529353
rs7529353
BCL2L15 ; AP4B1-AS1
1 1.000 0.120 1 113877840 3 prime UTR variant G/A snv 0.26 0.700 1.000 1 2009 2009