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: rs137853336
rs137853336
HNF4A
5 0.851 0.080 20 44413714 missense variant C/G;T snv 4.0E-06; 8.0E-05 0.800 1.000 4 1997 2007
dbSNP: rs137853338
rs137853338
HNF4A
1 1.000 0.080 20 44424243 missense variant T/G snv 0.800 1.000 4 1997 2007
dbSNP: rs1375557127
rs1375557127
HNF4A
2 0.925 0.080 20 44424123 missense variant G/A snv 4.0E-06 0.700 1.000 6 2000 2016
dbSNP: rs587777732
rs587777732
HNF4A ; MIR3646
9 0.763 0.240 20 44406195 missense variant C/T snv 0.700 1.000 6 2010 2017
dbSNP: rs1392795567
rs1392795567
HNF4A
2 0.925 0.080 20 44414663 splice donor variant G/A snv 0.700 1.000 4 1977 2013
dbSNP: rs1568724014
rs1568724014
HNF4A ; MIR3646
2 0.925 0.080 20 44407421 stop gained C/T snv 0.700 1.000 4 2000 2013
dbSNP: rs1385251852
rs1385251852
HNF4A ; MIR3646
2 0.925 0.080 20 44406208 frameshift variant G/- delins 0.700 1.000 1 2013 2013
dbSNP: rs1060499693
rs1060499693
HNF4A
1 1.000 0.080 20 44418482 missense variant T/A snv 0.700 0
dbSNP: rs1280663753
rs1280663753
HNF4A
1 1.000 0.080 20 44414548 inframe deletion AGA/- delins 0.700 0
dbSNP: rs137853334
rs137853334
HNF4A
1 1.000 0.080 20 44419813 stop gained C/G;T snv 0.700 0
dbSNP: rs137853335
rs137853335
HNF4A
1 1.000 0.080 20 44413795 stop gained C/T snv 0.700 0
dbSNP: rs1555816654
rs1555816654
HNF4A
1 1.000 0.080 20 44419790 missense variant T/C snv 0.700 0
dbSNP: rs1568731279
rs1568731279
HNF4A
3 0.925 0.160 20 44414506 splice acceptor variant G/A snv 0.700 0
dbSNP: rs193922469
rs193922469
HNF4A
1 1.000 0.080 20 44428368 missense variant C/A;G snv 4.0E-06 0.700 0
dbSNP: rs193922470
rs193922470
HNF4A
1 1.000 0.080 20 44428458 splice donor variant G/C snv 0.700 0
dbSNP: rs193922471
rs193922471
HNF4A ; MIR3646
1 1.000 0.080 20 44407437 frameshift variant GG/C delins 0.700 0
dbSNP: rs193922474
rs193922474
HNF4A
1 1.000 0.080 20 44414633 missense variant G/C snv 0.700 0
dbSNP: rs193922475
rs193922475
HNF4A
1 1.000 0.080 20 44414652 splice donor variant ACGACCAGGTGAGGATGG/- delins 0.700 0
dbSNP: rs193922476
rs193922476
HNF4A
1 1.000 0.080 20 44418502 frameshift variant GCT/TCAA delins 0.700 0
dbSNP: rs193922477
rs193922477
HNF4A
1 1.000 0.080 20 44419818 missense variant G/C snv 4.0E-06 4.2E-05 0.700 0
dbSNP: rs193922479
rs193922479
HNF4A
2 0.925 0.080 20 44424116 missense variant C/A;T snv 8.0E-06 7.0E-06 0.700 0
dbSNP: rs370239205
rs370239205
HNF4A
3 0.882 0.080 20 44413708 missense variant C/A;T snv 4.0E-05; 4.0E-06 0.010 1.000 1 2000 2000
dbSNP: rs749756893
rs749756893
ZNF436
1 1.000 0.080 1 23362583 stop gained G/A snv 4.0E-06 0.010 1.000 1 1998 1998
dbSNP: rs757863935
rs757863935
TMEM189 ; TMEM189-UBE2V1
1 1.000 0.080 20 50125072 stop gained G/A snv 0.010 1.000 1 1998 1998