Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2069718
rs2069718
IFNG ; IFNG-AS1
CUI: C0150988
Disease: Sclerodactyly
Sclerodactyly 		0.010 GeneticVariation BEFREE Raynaud's phenomenon, erosive arthritis, swollen hands and fingers, and sclerodactyly were significantly more frequently observed in MCTD patients with IFN-G rs2069718 G allele than in patients with IFN-G rs2069718 A allele. 31766529

2019