Source: CLINVAR

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: rs397517159
rs397517159
0.882 0.200 2 39007168 missense variant C/T snv
CUI: C0232466
Disease: Feeding difficulties
Feeding difficulties
0.700 1.000 3 2007 2007
dbSNP: rs1554389088
rs1554389088
0.807 0.160 7 44243526 missense variant G/A snv
CUI: C0232466
Disease: Feeding difficulties
Feeding difficulties
0.700 1.000 1 2017 2017
dbSNP: rs1554817910
rs1554817910
1.000 10 79216266 missense variant A/G snv
CUI: C0232466
Disease: Feeding difficulties
Feeding difficulties
0.700 1.000 1 2019 2019
dbSNP: rs752746786
rs752746786
0.742 0.560 1 1806503 missense variant A/C;G;T snv 4.0E-06
CUI: C0232466
Disease: Feeding difficulties
Feeding difficulties
0.700 1.000 1 2016 2016
dbSNP: rs772037717
rs772037717
0.882 0.080 6 98875675 missense variant A/G snv 1.2E-05 1.4E-05
CUI: C0232466
Disease: Feeding difficulties
Feeding difficulties
0.700 1.000 1 2016 2016
dbSNP: rs786200952
rs786200952
0.851 0.120 8 41934340 frameshift variant -/T delins
CUI: C0232466
Disease: Feeding difficulties
Feeding difficulties
0.700 1.000 1 2015 2015
dbSNP: rs867410737
rs867410737
0.708 0.440 19 1242559 missense variant C/T snv 6.7E-06
CUI: C0232466
Disease: Feeding difficulties
Feeding difficulties
0.700 1.000 1 2018 2018
dbSNP: rs869312823
rs869312823
0.882 0.080 1 1806509 missense variant T/C snv
CUI: C0232466
Disease: Feeding difficulties
Feeding difficulties
0.700 1.000 1 2016 2016
dbSNP: rs869312824
rs869312824
0.827 0.200 1 1804565 missense variant A/G snv
CUI: C0232466
Disease: Feeding difficulties
Feeding difficulties
0.700 1.000 1 2016 2016
dbSNP: rs1057518681
rs1057518681
0.827 0.200 8 143816821 splice acceptor variant T/C snv
CUI: C0232466
Disease: Feeding difficulties
Feeding difficulties
0.700 0
dbSNP: rs1057518879
rs1057518879
0.776 0.280 1 11965571 stop gained G/A snv
CUI: C0232466
Disease: Feeding difficulties
Feeding difficulties
0.700 0
dbSNP: rs1064795760
rs1064795760
0.882 0.080 9 92719007 inframe deletion ATT/- del
CUI: C0232466
Disease: Feeding difficulties
Feeding difficulties
0.700 0
dbSNP: rs1085307132
rs1085307132
0.882 0.160 8 143817668 frameshift variant -/TTTT delins
CUI: C0232466
Disease: Feeding difficulties
Feeding difficulties
0.700 0
dbSNP: rs1085307138
rs1085307138
0.807 0.160 8 143817591 splice donor variant C/T snv
CUI: C0232466
Disease: Feeding difficulties
Feeding difficulties
0.700 0
dbSNP: rs1085307139
rs1085307139
0.925 0.040 8 143817380 frameshift variant -/C delins
CUI: C0232466
Disease: Feeding difficulties
Feeding difficulties
0.700 0
dbSNP: rs1085307993
rs1085307993
0.716 0.440 5 161331056 missense variant C/T snv
CUI: C0232466
Disease: Feeding difficulties
Feeding difficulties
0.700 0
dbSNP: rs1114167294
rs1114167294
0.925 6 41587455 frameshift variant T/- del
CUI: C0232466
Disease: Feeding difficulties
Feeding difficulties
0.700 0
dbSNP: rs1218912272
rs1218912272
0.925 0.160 1 152314342 stop gained T/A snv 4.0E-06
CUI: C0232466
Disease: Feeding difficulties
Feeding difficulties
0.700 0
dbSNP: rs1344172059
rs1344172059
0.882 0.080 11 17430838 missense variant C/T snv 7.0E-06
CUI: C0232466
Disease: Feeding difficulties
Feeding difficulties
0.700 0
dbSNP: rs1345176461
rs1345176461
0.716 0.240 14 77027231 stop gained G/A;T snv 4.3E-06
CUI: C0232466
Disease: Feeding difficulties
Feeding difficulties
0.700 0
dbSNP: rs1380822792
rs1380822792
0.882 0.080 4 139336933 frameshift variant CTTGA/- delins
CUI: C0232466
Disease: Feeding difficulties
Feeding difficulties
0.700 0
dbSNP: rs139632595
rs139632595
0.807 0.160 4 121801465 missense variant T/C snv 6.0E-05 2.5E-04
CUI: C0232466
Disease: Feeding difficulties
Feeding difficulties
0.700 0
dbSNP: rs141322087
rs141322087
0.851 0.160 11 17404552 missense variant C/T snv 1.2E-05 2.1E-05
CUI: C0232466
Disease: Feeding difficulties
Feeding difficulties
0.700 0
dbSNP: rs146539065
rs146539065
0.752 0.240 4 25145092 synonymous variant C/T snv 2.8E-05 4.2E-05
CUI: C0232466
Disease: Feeding difficulties
Feeding difficulties
0.700 0
dbSNP: rs1554317002
rs1554317002
0.724 0.440 7 39950821 frameshift variant C/- delins
CUI: C0232466
Disease: Feeding difficulties
Feeding difficulties
0.700 0