ITGAM, integrin subunit alpha M, 3684

N. diseases: 343; N. variants: 14
Disease: Systemic Scleroderma ×
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: rs11860650
rs11860650 		0.882 0.120 16 31315385 intron variant C/T snv 0.14
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma 		Skin and Connective Tissue Diseases 0.800 1.000 1 2013 2013
dbSNP: rs2359661
rs2359661 		1.000 0.040 16 31269826 intron variant A/G snv 0.48
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma 		Skin and Connective Tissue Diseases 0.700 1.000 1 2013 2013
dbSNP: rs7190018
rs7190018 		1.000 0.040 16 31290157 intron variant G/A;C snv
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma 		Skin and Connective Tissue Diseases 0.700 1.000 1 2013 2013
dbSNP: rs1143679
rs1143679 		0.732 0.520 16 31265490 missense variant G/A snv 9.7E-02 0.11
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma 		Skin and Connective Tissue Diseases 0.010 1.000 1 2012 2012