LEPR, leptin receptor, 3953

N. diseases: 416; N. variants: 57
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10889569
rs10889569
1 65620511 intron variant A/T snv 0.46
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.800 1.000 2 2013 2019
dbSNP: rs1303050393
rs1303050393
1.000 1 65618108 missense variant T/C snv 4.0E-06
CUI: C3554225
Disease: LEPTIN RECEPTOR DEFICIENCY
LEPTIN RECEPTOR DEFICIENCY
0.700 1.000 2 1998 2015
dbSNP: rs11208662
rs11208662
1 65521481 intron variant G/C;T snv
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 1 2019 2019
dbSNP: rs17127608
rs17127608
1 65428258 intron variant C/T snv 4.2E-02
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs17127608
rs17127608
1 65428258 intron variant C/T snv 4.2E-02
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs201721079
rs201721079
1 65615104 intron variant -/C delins
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.700 1.000 1 2013 2013
dbSNP: rs34499590
rs34499590
1 65616108 missense variant C/G;T snv 2.5E-03
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs34499590
rs34499590
1 65616108 missense variant C/G;T snv 2.5E-03
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012
dbSNP: rs34499590
rs34499590
1 65616108 missense variant C/G;T snv 2.5E-03
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs35308591
rs35308591
1 65615104 intron variant -/C delins
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.700 1.000 1 2013 2013
dbSNP: rs369475236
rs369475236
1 65570514 missense variant A/G snv 4.0E-06; 2.8E-05 4.9E-05
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.010 1.000 1 2004 2004
dbSNP: rs3790438
rs3790438
1 65619842 intron variant T/A;G snv 0.18
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs4655537
rs4655537
1 65593118 intron variant A/G;T snv
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.700 1.000 1 2013 2013
dbSNP: rs4655555
rs4655555
1 65614586 intron variant T/A snv 0.20
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.700 1.000 1 2013 2013
dbSNP: rs4655557
rs4655557
1 65615104 intron variant T/A;C snv
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.700 1.000 1 2013 2013
dbSNP: rs61779781
rs61779781
1 65468671 intron variant T/C snv 0.30
CUI: C1314691
Disease: Age at menarche
Age at menarche
Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs6588153
rs6588153
1 65626334 intron variant T/A snv 0.43
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.700 1.000 1 2013 2013
dbSNP: rs6658330
rs6658330
1 65622146 intron variant T/A snv 0.25
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs6678033
rs6678033
1 65611941 intron variant G/A snv 0.46
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.700 1.000 1 2013 2013
dbSNP: rs6690625
rs6690625
1 65611907 intron variant T/G snv 0.28
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.700 1.000 1 2013 2013
dbSNP: rs67129560
rs67129560
1 65440446 intron variant A/G snv 0.54
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.700 1.000 1 2018 2018
dbSNP: rs72683129
rs72683129
1 65604098 intron variant A/G snv 9.4E-02
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.700 1.000 1 2018 2018
dbSNP: rs7516341
rs7516341
1 65622460 intron variant T/C snv 0.46
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.700 1.000 1 2013 2013
dbSNP: rs9436735
rs9436735
1 65419378 upstream gene variant C/G snv 2.5E-02
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs9436735
rs9436735
1 65419378 upstream gene variant C/G snv 2.5E-02
High density lipoprotein measurement
0.700 1.000 1 2012 2012