SCMH1, Scm polycomb group protein homolog 1, 22955

N. diseases: 11; N. variants: 11
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: rs2885697
rs2885697 		1.000 0.080 1 41078607 intron variant G/T snv 0.72
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.700 1.000 2 2018 2018
dbSNP: rs1032728
rs1032728 		1 41213894 intron variant A/T snv 0.17
CUI: C1314691
Disease: Age at menarche
Age at menarche 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs11209718
rs11209718 		1 41223266 intron variant C/G;T snv
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2013 2013
dbSNP: rs11209718
rs11209718 		1 41223266 intron variant C/G;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2013 2013
dbSNP: rs1140227
rs1140227 		1 41028139 3 prime UTR variant C/T snv 0.10
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs114233776
rs114233776 		1 41152625 missense variant G/A snv 4.7E-03 4.7E-03
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs12024115
rs12024115 		1 41068685 intron variant C/T snv 0.11
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs2284801
rs2284801 		1 41158056 intron variant G/C snv 0.18
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs2749418
rs2749418 		1 41044002 intron variant T/C snv 0.69
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019
dbSNP: rs2885697
rs2885697 		1.000 0.080 1 41078607 intron variant G/T snv 0.72
CUI: C0424678
Disease: Lean body mass
Lean body mass 		0.700 1.000 1 2019 2019
dbSNP: rs35613919
rs35613919 		1 41174805 intron variant C/T snv 1.9E-02
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs6600365
rs6600365 		1 41090581 intron variant C/T snv 0.65
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2014 2014
dbSNP: rs6686842
rs6686842 		1 41065199 intron variant T/C snv 0.65
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2008 2008
dbSNP: rs6686842
rs6686842 		1 41065199 intron variant T/C snv 0.65
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2008 2008