RHOC, ras homolog family member C, 389

N. diseases: 50; N. variants: 3
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: rs11102522
rs11102522 		1.000 0.040 1 112708266 intron variant T/C snv 0.19
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma 		Skin and Connective Tissue Diseases 0.010 1.000 1 2016 2016
dbSNP: rs11538960
rs11538960 		1.000 0.040 1 112701565 missense variant C/T snv 4.2E-04 5.2E-04
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma 		Skin and Connective Tissue Diseases 0.010 1.000 1 2016 2016