RMC1, regulator of MON1-CCZ1, 29919

N. diseases: 110; N. variants: 6
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: rs1808579
rs1808579 		18 23524924 intron variant C/T snv 0.47
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 4 2015 2019
dbSNP: rs1788820
rs1788820 		18 23521980 intron variant A/G snv 0.69
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 2 2017 2018
dbSNP: rs177430
rs177430 		18 23506161 intron variant C/A;T snv
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs177430
rs177430 		18 23506161 intron variant C/A;T snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2017 2017
dbSNP: rs177430
rs177430 		18 23506161 intron variant C/A;T snv
CUI: C0562350
Disease: Hip circumference
Hip circumference 		0.700 1.000 1 2017 2017
dbSNP: rs177430
rs177430 		18 23506161 intron variant C/A;T snv
CUI: C0005910
Disease: Body Weight
Body Weight 		Pathological Conditions, Signs and Symptoms 0.700 1.000 1 2017 2017
dbSNP: rs1788808
rs1788808 		18 23510059 intron variant A/C;G snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs1808579
rs1808579 		18 23524924 intron variant C/T snv 0.47
CUI: C0037369
Disease: Smoking
Smoking 		Behavior and Behavior Mechanisms 0.700 1.000 1 2017 2017
dbSNP: rs1808579
rs1808579 		18 23524924 intron variant C/T snv 0.47
CUI: C0562350
Disease: Hip circumference
Hip circumference 		0.700 1.000 1 2015 2015
dbSNP: rs8086463
rs8086463 		18 23532038 3 prime UTR variant A/G snv 1.1E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2012 2012
dbSNP: rs8086463
rs8086463 		18 23532038 3 prime UTR variant A/G snv 1.1E-02
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs8086463
rs8086463 		18 23532038 3 prime UTR variant A/G snv 1.1E-02
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs891387
rs891387 		18 23523945 intron variant T/C snv 0.55
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2019 2019
dbSNP: rs891387
rs891387 		18 23523945 intron variant T/C snv 0.55
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019