RBM6, RNA binding motif protein 6, 10180

N. diseases: 28; N. variants: 12
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: rs2013208
rs2013208 		3 50091966 intron variant C/T snv 0.61 0.56
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 3 2013 2019
dbSNP: rs6762477
rs6762477 		3 50055776 intron variant G/A snv 0.64
CUI: C1314691
Disease: Age at menarche
Age at menarche 		Behavior and Behavior Mechanisms 0.800 1.000 2 2010 2014
dbSNP: rs11130226
rs11130226 		3 49955758 intron variant T/G snv 0.48
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs111439884
rs111439884 		3 49986605 intron variant A/C snv 0.47
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2018 2018
dbSNP: rs149787889
rs149787889 		3 50074623 intron variant G/A snv 1.2E-02
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2017 2017
dbSNP: rs1986599
rs1986599 		3 49997204 intron variant T/G snv 7.9E-02
CUI: C0424621
Disease: Body Fat Distribution
Body Fat Distribution 		0.700 1.000 1 2019 2019
dbSNP: rs2013208
rs2013208 		3 50091966 intron variant C/T snv 0.61 0.56
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs2013208
rs2013208 		3 50091966 intron variant C/T snv 0.61 0.56
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2013 2013
dbSNP: rs2013208
rs2013208 		3 50091966 intron variant C/T snv 0.61 0.56
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs2240328
rs2240328 		3 50075571 intron variant T/A;C snv
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2018 2018
dbSNP: rs2624816
rs2624816 		3 50079879 intron variant T/G snv 0.53
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs35012435
rs35012435 		3 49994407 intron variant C/T snv 0.22
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs35849525
rs35849525 		3 50029917 intron variant T/C snv 0.22
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs4688756
rs4688756 		1.000 0.040 3 50002761 intron variant T/A snv 0.44
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs4688756
rs4688756 		1.000 0.040 3 50002761 intron variant T/A snv 0.44
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 1 2019 2019
dbSNP: rs62262139
rs62262139 		1.000 0.040 3 49984616 intron variant G/A;C snv
CUI: C0029408
Disease: Degenerative polyarthritis
Degenerative polyarthritis 		Musculoskeletal Diseases 0.700 1.000 1 2019 2019