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: rs120074160
rs120074160
0.925 7 66994286 stop gained T/A snv 1.7E-04 1.0E-03
CUI: C0349588
Disease: Short stature
Short stature
0.700 0
dbSNP: rs200635937
rs200635937
0.925 0.040 1 168104855 missense variant A/T snv 2.9E-03 8.0E-04
CUI: C0349588
Disease: Short stature
Short stature
0.700 0
dbSNP: rs202070666
rs202070666
X 154460239 missense variant G/A snv 2.2E-04 6.5E-04
CUI: C0349588
Disease: Short stature
Short stature
0.700 0
dbSNP: rs188675529
rs188675529
0.827 0.240 16 67842794 missense variant C/G;T snv 1.6E-03 6.0E-04
CUI: C0349588
Disease: Short stature
Short stature
0.700 0
dbSNP: rs201431517
rs201431517
0.827 0.200 15 65021533 missense variant G/A snv 3.5E-04 5.7E-04
CUI: C0349588
Disease: Short stature
Short stature
0.700 1.000 2 2011 2014
dbSNP: rs80338903
rs80338903
0.701 0.360 1 216247095 frameshift variant C/- del 7.6E-04 5.4E-04
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: rs1801175
rs1801175
0.807 0.240 17 42903947 missense variant C/T snv 5.7E-04 3.4E-04
CUI: C0349588
Disease: Short stature
Short stature
0.700 0
dbSNP: rs138249161
rs138249161
0.827 0.240 12 106432421 missense variant T/A snv 2.7E-04 3.0E-04
CUI: C0349588
Disease: Short stature
Short stature
0.700 0
dbSNP: rs139632595
rs139632595
0.807 0.160 4 121801465 missense variant T/C snv 6.0E-05 2.5E-04
CUI: C0349588
Disease: Short stature
Short stature
0.700 0
dbSNP: rs143814221
rs143814221
GHR
0.882 0.160 5 42711306 missense variant T/C snv 2.7E-04 2.3E-04
CUI: C0349588
Disease: Short stature
Short stature
0.700 0
dbSNP: rs376253982
rs376253982
X 48966313 splice region variant C/A snv 2.0E-04 2.1E-04
CUI: C0349588
Disease: Short stature
Short stature
0.700 0
dbSNP: rs202160208
rs202160208
0.827 0.160 3 49722056 missense variant C/T snv 2.9E-04 1.8E-04
CUI: C0349588
Disease: Short stature
Short stature
0.700 0
dbSNP: rs767539150
rs767539150
12 71656953 missense variant C/T snv 1.8E-04 1.7E-04
CUI: C0349588
Disease: Short stature
Short stature
0.700 0
dbSNP: rs119473033
rs119473033
0.827 0.320 2 216478216 stop gained G/T snv 8.0E-05 1.3E-04
CUI: C0349588
Disease: Short stature
Short stature
0.700 0
dbSNP: rs141844660
rs141844660
6 99443648 stop gained C/A snv 1.3E-04 1.2E-04
CUI: C0349588
Disease: Short stature
Short stature
0.700 0
dbSNP: rs148723879
rs148723879
10 69246212 missense variant C/T snv 9.9E-05 1.2E-04
CUI: C0349588
Disease: Short stature
Short stature
0.700 0
dbSNP: rs370433088
rs370433088
20 62322314 missense variant C/T snv 1.0E-04 1.0E-04
CUI: C0349588
Disease: Short stature
Short stature
0.700 0
dbSNP: rs377035972
rs377035972
14 24155679 missense variant G/A snv 5.6E-05 9.8E-05
CUI: C0349588
Disease: Short stature
Short stature
0.700 0
dbSNP: rs189150283
rs189150283
0.925 22 20992304 stop gained C/T snv 6.0E-05 7.0E-05
CUI: C0349588
Disease: Short stature
Short stature
0.700 0
dbSNP: rs149830411
rs149830411
0.827 0.360 17 46171276 stop gained G/A snv 5.2E-05 5.6E-05
CUI: C0349588
Disease: Short stature
Short stature
0.700 0
dbSNP: rs771172991
rs771172991
20 34987284 splice donor variant AG/- delins 5.6E-05
CUI: C0349588
Disease: Short stature
Short stature
0.700 0
dbSNP: rs766464011
rs766464011
20 62333128 missense variant G/T snv 1.1E-04 5.6E-05
CUI: C0349588
Disease: Short stature
Short stature
0.700 0
dbSNP: rs201430951
rs201430951
0.925 0.040 14 31599308 missense variant T/C snv 1.5E-04 5.6E-05
CUI: C0349588
Disease: Short stature
Short stature
0.700 0
dbSNP: rs747141054
rs747141054
8 42973316 missense variant G/A snv 2.4E-05 4.9E-05
CUI: C0349588
Disease: Short stature
Short stature
0.700 0