rs1131690789, RBM10

N. diseases: 2
Source: CLINVAR ×
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.
Dysmorphic features
CUI: C0432072
Disease: Dysmorphic features
611 1.000 X 47181316 frameshift variant AG/- delins 0.700 0
Multiple congenital anomalies
CUI: C0000772
Disease: Multiple congenital anomalies
350 1.000 X 47181316 frameshift variant AG/- delins 0.700 0