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: 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: rs864309503
rs864309503
0.882 0.200 22 30941503 missense variant G/A snv
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
0.700 1.000 10 2016 2017
dbSNP: rs1555087619
rs1555087619
11 72308526 splice donor variant C/T snv
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
0.700 1.000 4 2015 2015
dbSNP: rs797044806
rs797044806
0.925 17 50354465 frameshift variant -/C delins
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
0.700 1.000 4 2015 2018
dbSNP: rs137853063
rs137853063
0.882 0.080 14 96876033 stop gained C/G;T snv 6.4E-05; 4.0E-06
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
0.700 1.000 1 2015 2015
dbSNP: rs398123009
rs398123009
0.790 0.200 11 66211206 missense variant C/T snv 7.0E-06
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
0.700 1.000 1 2015 2015
dbSNP: rs786205154
rs786205154
1.000 0.120 12 11885921 coding sequence variant GAACA/- delins
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
0.700 1.000 1 2015 2015
dbSNP: rs797044859
rs797044859
6 157200765 frameshift variant AT/- del
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
0.700 1.000 1 2015 2015
dbSNP: rs797044890
rs797044890
16 89275092 splice donor variant C/T snv
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
0.700 1.000 1 2015 2015
dbSNP: rs797044919
rs797044919
8 60845364 frameshift variant -/C delins
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
0.700 1.000 1 2015 2015
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: rs777218310
rs777218310
0.925 10 133369907 frameshift variant TA/- delins 1.6E-05 1.3E-04
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
0.700 1.000 14 2014 2018
dbSNP: rs587777695
rs587777695
0.925 0.120 5 61544156 missense variant C/T snv
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
0.700 1.000 3 2014 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: rs1462161137
rs1462161137
1.000 17 76733042 frameshift variant -/A delins 7.0E-06
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
0.700 1.000 2 2014 2014
dbSNP: rs1554865146
rs1554865146
10 100809207 stop gained C/G snv
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
0.700 1.000 1 2014 2014
dbSNP: rs1341894581
rs1341894581
0.925 2 232486499 frameshift variant ACCGGGCCCCGGTGGCGCTGCGCGCAGCGCCCAACGGGAAGCCCGG/- delins 3.3E-04 1.1E-04
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
0.700 1.000 5 2013 2015
dbSNP: rs1555933851
rs1555933851
1.000 X 64919152 frameshift variant -/G delins
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
0.700 1.000 2 2013 2015
dbSNP: rs797044863
rs797044863
1.000 X 64921894 stop gained G/A snv
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
0.700 1.000 2 2013 2015
dbSNP: rs746765465
rs746765465
1.000 17 40089359 frameshift variant C/- delins
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
0.700 1.000 9 2012 2016
dbSNP: rs1555465942
rs1555465942
1.000 16 30737415 frameshift variant C/- delins
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
0.700 1.000 8 2012 2016
dbSNP: rs1057517825
rs1057517825
0.925 22 23834143 missense variant G/A snv
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
0.700 1.000 5 2012 2014
dbSNP: rs1376334317
rs1376334317
0.925 3 136473546 missense variant C/T snv
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
0.700 1.000 5 2012 2017
dbSNP: rs1555574888
rs1555574888
1.000 17 46170875 frameshift variant G/- delins
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
0.700 1.000 5 2012 2016
dbSNP: rs1554274371
rs1554274371
6 142753484 stop gained G/A snv
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
0.700 1.000 4 2012 2016