rs1569551861, FLNA

N. diseases: 4
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
OTOPALATODIGITAL SYNDROME, TYPE II
CUI: C1844696
Disease: OTOPALATODIGITAL SYNDROME, TYPE II
0.700 CausalMutation CLINVAR
Melnick-Needles Syndrome
CUI: C0025237
Disease: Melnick-Needles Syndrome
0.700 CausalMutation CLINVAR
Periventricular Heterotopia, X-Linked
CUI: C1848213
Disease: Periventricular Heterotopia, X-Linked
0.700 CausalMutation CLINVAR
Frontometaphyseal dysplasia
CUI: C0265293
Disease: Frontometaphyseal dysplasia
0.700 CausalMutation CLINVAR