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: rs10174238
rs10174238
0.724 0.200 2 191108308 intron variant G/A snv 0.70
CUI: C0748540
Disease: Scleroderma, Limited
Scleroderma, Limited
Skin and Connective Tissue Diseases 0.700 1.000 1 2018 2018
dbSNP: rs11893432
rs11893432
0.827 0.120 2 191057148 intron variant C/G snv 0.21
CUI: C0748540
Disease: Scleroderma, Limited
Scleroderma, Limited
Skin and Connective Tissue Diseases 0.700 1.000 1 2018 2018