Gene: HNF4A ×
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: rs4812829
rs4812829
HNF4A
3 0.925 0.120 20 44360627 intron variant G/A snv 0.18 0.830 1.000 7 2011 2017
dbSNP: rs1800961
rs1800961
HNF4A
21 0.851 0.160 20 44413724 missense variant C/T snv 3.1E-02 2.5E-02 0.720 1.000 4 2010 2019
dbSNP: rs137853337
rs137853337
HNF4A
1 1.000 0.080 20 44428409 missense variant G/A snv 8.0E-06; 8.0E-06 7.0E-06 0.700 1.000 1 1998 1998
dbSNP: rs16988991
rs16988991
HNF4A
1 1.000 0.080 20 44361137 intron variant G/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs4810426
rs4810426
HNF4A ; HNF4A-AS1
1 1.000 0.080 20 44373081 intron variant C/T snv 0.14 0.700 1.000 1 2018 2018
dbSNP: rs4812831
rs4812831
HNF4A ; HNF4A-AS1
1 1.000 0.080 20 44389620 intron variant G/A snv 0.12 0.700 1.000 1 2011 2011
dbSNP: rs6103716
rs6103716
HNF4A
1 1.000 0.080 20 44370990 intron variant A/C snv 0.37 0.700 1.000 1 2019 2019
dbSNP: rs587777732
rs587777732
HNF4A ; MIR3646
9 0.763 0.240 20 44406195 missense variant C/T snv 0.700 0
dbSNP: rs2144908
rs2144908
HNF4A ; LOC105372629
5 0.851 0.120 20 44357077 intron variant G/A snv 0.18 0.100 1.000 10 2006 2019
dbSNP: rs952497863
rs952497863
HNF4A
4 0.925 0.080 20 44414511 missense variant C/T snv 0.070 1.000 7 2003 2017
dbSNP: rs1223493898
rs1223493898
HNF4A
5 0.851 0.120 20 44406090 missense variant G/A;C snv 0.050 1.000 5 2005 2012
dbSNP: rs2071197
rs2071197
HNF4A
2 0.925 0.120 20 44401795 intron variant G/A snv 0.11 0.030 1.000 3 2005 2011
dbSNP: rs3212183
rs3212183
HNF4A ; MIR3646
2 0.925 0.080 20 44406498 intron variant C/T snv 0.58 0.030 0.667 3 2005 2017
dbSNP: rs1885088
rs1885088
HNF4A
2 1.000 0.080 20 44410400 intron variant G/A snv 0.15 0.020 1.000 2 2009 2017
dbSNP: rs753285226
rs753285226
HNF4A
5 0.882 0.080 20 44406084 missense variant C/A;T snv 4.0E-06 0.020 1.000 2 2008 2016
dbSNP: rs763010207
rs763010207
HNF4A
3 0.925 0.080 20 44414531 missense variant A/G snv 4.0E-06 1.4E-05 0.020 1.000 2 2000 2001
dbSNP: rs1031647179
rs1031647179
HNF4A
1 1.000 0.080 20 44424278 missense variant C/G;T snv 0.010 1.000 1 2008 2008
dbSNP: rs1159931590
rs1159931590
HNF4A
1 1.000 0.080 20 44414655 missense variant A/G snv 4.3E-06 0.010 1.000 1 1999 1999
dbSNP: rs1486917678
rs1486917678
HNF4A
1 1.000 0.080 20 44424101 missense variant C/T snv 7.0E-06 0.010 1.000 1 1999 1999
dbSNP: rs148745312
rs148745312
HNF4A
1 1.000 0.080 20 44428431 missense variant C/A;T snv 4.0E-06; 4.0E-06 0.010 1.000 1 2019 2019
dbSNP: rs200985945
rs200985945
HNF4A
2 0.925 0.080 20 44419772 missense variant G/A;T snv 4.0E-06 0.010 < 0.001 1 2015 2015
dbSNP: rs201749293
rs201749293
HNF4A
1 1.000 0.080 20 44414649 missense variant C/T snv 1.7E-04 1.0E-04 0.010 1.000 1 2015 2015
dbSNP: rs2425637
rs2425637
HNF4A ; HNF4A-AS1
3 0.925 0.080 20 44395409 intron variant G/T snv 0.42 0.010 < 0.001 1 2010 2010
dbSNP: rs2425640
rs2425640
HNF4A
1 1.000 0.080 20 44399397 intron variant A/G snv 0.63 0.010 1.000 1 2004 2004
dbSNP: rs3212198
rs3212198
HNF4A
1 1.000 0.080 20 44415722 intron variant C/G;T snv 0.010 1.000 1 2008 2008