Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1340611668
rs1340611668
1 210348976 start lost A/G;T snv 7.0E-06
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
0.700 1.000 4 2004 2014
dbSNP: rs1553249737
rs1553249737
1.000 1 165743263 stop gained G/T snv
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
0.700 1.000 4 2010 2014
dbSNP: rs1026300967
rs1026300967
1.000 1 156868246 missense variant T/C snv
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
0.700 1.000 3 2012 2017
dbSNP: rs1553173425
rs1553173425
1 1338112 frameshift variant G/- delins
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
0.700 1.000 3 2007 2015
dbSNP: rs1553263326
rs1553263326
1.000 1 156881446 intron variant G/A snv
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
0.700 1.000 3 2012 2017
dbSNP: rs797044857
rs797044857
1 24354474 missense variant C/G snv
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
0.700 1.000 3 2014 2018
dbSNP: rs864309703
rs864309703
1.000 0.200 1 147908106 missense variant G/A;C;T snv
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
0.700 1.000 3 2010 2017
dbSNP: rs1553284965
rs1553284965
1 92833459 splice donor variant G/A snv
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
0.700 1.000 1 2008 2008
dbSNP: rs1553353206
rs1553353206
1.000 1 224398525 frameshift variant CATTTAACAA/- delins
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
0.700 1.000 1 2017 2017
dbSNP: rs869312953
rs869312953
0.851 0.120 1 64846735 missense variant G/T snv
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
0.700 1.000 1 2015 2015
dbSNP: rs147001633
rs147001633
0.776 0.240 2 25234373 missense variant C/A;G;T snv 4.0E-06; 4.0E-06; 2.2E-04
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
0.700 1.000 36 1989 2018
dbSNP: rs1553521389
rs1553521389
1.000 2 224503679 frameshift variant AG/- delins
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
0.700 1.000 25 1986 2016
dbSNP: rs1057521083
rs1057521083
0.925 0.200 2 199348709 missense variant G/A snv
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
0.700 1.000 21 1989 2017
dbSNP: rs137852813
rs137852813
0.807 0.200 2 39051202 missense variant A/C;G snv
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
0.700 1.000 21 2002 2016
dbSNP: rs1553551705
rs1553551705
1.000 2 199349065 frameshift variant GT/- delins
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
0.700 1.000 21 1989 2017
dbSNP: rs397517172
rs397517172
0.925 0.160 2 39056704 missense variant T/C snv
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
0.700 1.000 21 2002 2016
dbSNP: rs397517174
rs397517174
0.925 0.160 2 39054822 missense variant A/C;G snv
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
0.700 1.000 21 2002 2016
dbSNP: rs672601370
rs672601370
0.790 0.160 2 240775863 missense variant G/A snv
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
0.700 1.000 15 2011 2018
dbSNP: rs1553485330
rs1553485330
2 178531129 frameshift variant C/- delins
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
0.700 1.000 14 1991 2014
dbSNP: rs1553650442
rs1553650442
0.925 0.160 2 178593732 frameshift variant C/-;CCC delins
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
0.700 1.000 14 1991 2014
dbSNP: rs201553266
rs201553266
NEB
0.882 0.080 2 151551738 splice region variant C/T snv 2.8E-05 7.0E-06
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
0.700 1.000 12 1988 2017
dbSNP: rs755531536
rs755531536
NEB
0.925 0.080 2 151694370 frameshift variant C/- del 7.0E-06
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
0.700 1.000 12 1988 2017
dbSNP: rs1553518509
rs1553518509
1.000 0.040 2 148468916 stop gained C/T snv
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
0.700 1.000 11 2007 2016
dbSNP: rs121964881
rs121964881
1.000 2 70958103 missense variant G/A snv 2.0E-05 9.1E-05
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
0.700 1.000 9 1995 2017
dbSNP: rs782138777
rs782138777
1.000 0.280 2 70958399 stop gained C/T snv 1.2E-05 1.4E-05
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
0.700 1.000 9 1995 2017