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: rs1561892336
rs1561892336
0.807 0.200 6 43050050 stop gained C/T snv
CUI: C0349588
Disease: Short stature
Short stature
0.700 1.000 1 2019 2019
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: rs1555954284
rs1555954284
0.752 0.360 X 41346607 missense variant C/T snv
CUI: C0349588
Disease: Short stature
Short stature
0.700 0
dbSNP: rs1557853919
rs1557853919
1 153939040 missense variant G/A snv
CUI: C0349588
Disease: Short stature
Short stature
0.700 0
dbSNP: rs1057519436
rs1057519436
0.882 0.200 3 47846550 missense variant G/A snv
CUI: C0349588
Disease: Short stature
Short stature
0.700 0
dbSNP: rs753242774
rs753242774
0.882 0.120 3 47848237 missense variant C/A;T snv
CUI: C0349588
Disease: Short stature
Short stature
0.700 0
dbSNP: rs1057518834
rs1057518834
DMD
X 32849737 frameshift variant C/- delins
CUI: C0349588
Disease: Short stature
Short stature
0.700 0
dbSNP: rs768564744
rs768564744
17 78525107 missense variant C/G;T snv 4.0E-06; 4.0E-05
CUI: C0349588
Disease: Short stature
Short stature
0.700 0
dbSNP: rs763505389
rs763505389
17 78491549 missense variant C/T snv 1.6E-05 7.0E-06
CUI: C0349588
Disease: Short stature
Short stature
0.700 0
dbSNP: rs771063992
rs771063992
0.827 0.240 5 34937431 stop gained C/T snv 2.8E-05 2.8E-05
CUI: C0349588
Disease: Short stature
Short stature
0.700 0
dbSNP: rs757167361
rs757167361
0.925 17 2030171 missense variant T/A;C;G snv
CUI: C0349588
Disease: Short stature
Short stature
0.700 0
dbSNP: rs201435914
rs201435914
19 53636878 stop gained C/T snv 3.5E-04 3.6E-04
CUI: C0349588
Disease: Short stature
Short stature
0.700 0
dbSNP: rs1064796765
rs1064796765
0.763 0.240 14 102002950 missense variant G/A snv
CUI: C0349588
Disease: Short stature
Short stature
0.700 0
dbSNP: rs1567010427
rs1567010427
0.882 14 102010824 missense variant G/A snv
CUI: C0349588
Disease: Short stature
Short stature
0.700 0
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: 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: rs1569355102
rs1569355102
0.695 0.360 21 37472869 frameshift variant TAAC/- delins
CUI: C0349588
Disease: Short stature
Short stature
0.700 0
dbSNP: rs724159949
rs724159949
0.827 0.240 21 37486563 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: rs797044523
rs797044523
0.882 21 37480756 frameshift variant -/A 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: rs587776917
rs587776917
0.776 0.200 2 232485937 stop gained -/T delins
CUI: C0349588
Disease: Short stature
Short stature
0.700 0