PDGFC, platelet derived growth factor C, 56034

N. diseases: 69; N. variants: 9
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: rs10517653
rs10517653
4 156812838 intron variant G/A;T snv 0.14
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2019 2019
dbSNP: rs10517660
rs10517660
4 156921244 intron variant A/G snv 0.50
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2019 2019
dbSNP: rs11100083
rs11100083
4 156761446 3 prime UTR variant T/C snv 0.39
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio
0.700 1.000 1 2019 2019
dbSNP: rs113128512
rs113128512
4 156761036 3 prime UTR variant T/C snv 6.7E-02
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement
0.700 1.000 1 2016 2016
dbSNP: rs4691380
rs4691380
4 156798972 intron variant C/T snv 0.45
CUI: C0578022
Disease: Finding of body mass index
Finding of body mass index
0.700 1.000 1 2012 2012
dbSNP: rs4691380
rs4691380
4 156798972 intron variant C/T snv 0.45
CUI: C0005893
Disease: Body mass index procedure
Body mass index procedure
0.700 1.000 1 2012 2012
dbSNP: rs4691380
rs4691380
4 156798972 intron variant C/T snv 0.45
High density lipoprotein measurement
0.700 1.000 1 2018 2018
dbSNP: rs4691380
rs4691380
4 156798972 intron variant C/T snv 0.45
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2012 2012
dbSNP: rs6822892
rs6822892
4 156813523 intron variant A/C;G snv
High density lipoprotein measurement
0.700 1.000 1 2017 2017
dbSNP: rs76488803
rs76488803
4 156849119 intron variant G/A snv 6.1E-02
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs7657225
rs7657225
0.925 0.040 4 156815383 intron variant T/C snv 6.7E-02
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis
Musculoskeletal Diseases 0.700 1.000 1 2018 2018
dbSNP: rs7657225
rs7657225
0.925 0.040 4 156815383 intron variant T/C snv 6.7E-02
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
0.700 1.000 1 2018 2018
dbSNP: rs7672622
rs7672622
4 156784399 intron variant A/G snv 0.41
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2019 2019