rs72656387, COL1A2

N. diseases: 3
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
EHLERS-DANLOS SYNDROME, CLASSIC TYPE, 1
CUI: C4552122
Disease: EHLERS-DANLOS SYNDROME, CLASSIC TYPE, 1
81 0.882 0.120 7 94409367 missense variant G/A snv 8.0E-06 7.0E-06 0.700 1.000 8 1993 2017
Lobstein Disease
CUI: C0023931
Disease: Lobstein Disease
257 0.882 0.120 7 94409367 missense variant G/A snv 8.0E-06 7.0E-06 0.700 1.000 8 1993 2017
Osteogenesis Imperfecta
CUI: C0029434
Disease: Osteogenesis Imperfecta
91 0.882 0.120 7 94409367 missense variant G/A snv 8.0E-06 7.0E-06 0.700 0