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: rs1559155800
rs1559155800
1.000 0.200 2 219568150 missense variant C/T snv
CUI: C0349588
Disease: Short stature
Short stature
0.700 1.000 1 2019 2019
dbSNP: rs1561875767
rs1561875767
1.000 0.200 6 43041036 stop gained G/A snv
CUI: C0349588
Disease: Short stature
Short stature
0.700 1.000 1 2019 2019
dbSNP: rs1057518939
rs1057518939
1.000 0.040 8 99511424 frameshift variant A/- del
CUI: C0349588
Disease: Short stature
Short stature
0.700 0
dbSNP: rs1057519451
rs1057519451
1.000 0.120 14 78709310 missense variant A/G snv 1.4E-05
CUI: C0349588
Disease: Short stature
Short stature
0.700 0
dbSNP: rs121913115
rs121913115
1.000 0.120 4 1801928 missense variant A/G snv
CUI: C0349588
Disease: Short stature
Short stature
0.700 0
dbSNP: rs137852552
rs137852552
1.000 0.080 Y 641037 stop gained C/A;T snv
CUI: C0349588
Disease: Short stature
Short stature
0.700 0
dbSNP: rs1553538488
rs1553538488
1.000 0.200 2 219570542 frameshift variant -/G delins
CUI: C0349588
Disease: Short stature
Short stature
0.700 0
dbSNP: rs1555548680
rs1555548680
1.000 0.120 17 42216066 missense variant T/C snv
CUI: C0349588
Disease: Short stature
Short stature
0.700 0
dbSNP: rs1561002040
rs1561002040
1.000 4 139454380 frameshift variant C/- delins
CUI: C0349588
Disease: Short stature
Short stature
0.700 0
dbSNP: rs1565191262
rs1565191262
1.000 0.080 11 59125559 frameshift variant T/- del
CUI: C0349588
Disease: Short stature
Short stature
0.700 0
dbSNP: rs531047390
rs531047390
1.000 0.120 14 78968349 splice region variant A/G snv 2.0E-04 2.1E-05
CUI: C0349588
Disease: Short stature
Short stature
0.700 0
dbSNP: rs864309521
rs864309521
1.000 0.200 6 43043631 splice acceptor variant C/G snv
CUI: C0349588
Disease: Short stature
Short stature
0.700 0
dbSNP: rs1057516034
rs1057516034
0.925 0.120 5 37052453 stop gained C/T snv
CUI: C0349588
Disease: Short stature
Short stature
0.700 1.000 1 2016 2016
dbSNP: rs1057516037
rs1057516037
0.925 X 72464626 protein altering variant TGGAG/AC delins
CUI: C0349588
Disease: Short stature
Short stature
0.700 1.000 1 2016 2016
dbSNP: rs1561873941
rs1561873941
0.925 0.200 6 43040335 frameshift variant T/- del
CUI: C0349588
Disease: Short stature
Short stature
0.700 1.000 1 2019 2019
dbSNP: rs1561881909
rs1561881909
0.925 0.200 6 43044835 frameshift variant G/- delins
CUI: C0349588
Disease: Short stature
Short stature
0.700 1.000 1 2019 2019
dbSNP: rs760929207
rs760929207
0.925 0.200 2 219568050 splice donor variant ACCTTTGACTG/- delins 8.1E-06 7.0E-06
CUI: C0349588
Disease: Short stature
Short stature
0.700 1.000 1 2019 2019
dbSNP: rs797044519
rs797044519
0.925 21 37478285 stop gained C/A;G;T snv
CUI: C0349588
Disease: Short stature
Short stature
0.700 1.000 1 2015 2015
dbSNP: rs797044520
rs797044520
0.925 21 37505442 stop gained C/T snv
CUI: C0349588
Disease: Short stature
Short stature
0.700 1.000 1 2015 2015
dbSNP: rs797044521
rs797044521
0.925 21 37480768 frameshift variant A/- delins
CUI: C0349588
Disease: Short stature
Short stature
0.700 1.000 1 2015 2015
dbSNP: rs797044522
rs797044522
0.925 21 37496119 frameshift variant AGAT/- delins
CUI: C0349588
Disease: Short stature
Short stature
0.700 1.000 1 2015 2015
dbSNP: rs797044524
rs797044524
0.925 21 37486513 missense variant A/T snv
CUI: C0349588
Disease: Short stature
Short stature
0.700 1.000 1 2015 2015
dbSNP: rs797044525
rs797044525
0.925 21 37490244 missense variant T/G snv
CUI: C0349588
Disease: Short stature
Short stature
0.700 1.000 1 2015 2015
dbSNP: rs797044526
rs797044526
0.925 21 37490393 missense variant C/T snv
CUI: C0349588
Disease: Short stature
Short stature
0.700 1.000 1 2015 2015
dbSNP: rs1057518791
rs1057518791
0.925 0.120 8 115604739 stop gained C/T snv
CUI: C0349588
Disease: Short stature
Short stature
0.700 0