List of variants reported as pathogenic for Wagner syndrome by OMIM

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Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_004385.5(VCAN):c.4004-1G>A	rs80356554
NM_004385.5(VCAN):c.4004-1G>C	rs80356554
NM_004385.5(VCAN):c.4004-2A>G	rs80356555
NM_004385.5(VCAN):c.4004-2A>T	rs80356555
NM_004385.5(VCAN):c.4004-5T>A	rs80356556
NM_004385.5(VCAN):c.4004-5T>C	rs80356556
NM_004385.5(VCAN):c.9265+1G>A	rs80356553
NM_004385.5(VCAN):c.9265+2T>A	rs397515437

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