List of variants reported as uncertain significance for autosomal dominant Robinow syndrome 1 by Illumina Laboratory Services, Illumina

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Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_003392.7(WNT5A):c.*2711del	rs374459457	0.01120
NM_003392.7(WNT5A):c.547G>A (p.Gly183Ser)	rs1393089710	0.00001
NM_003392.6(WNT5A):c.-394_-392delCCA	rs886058749
NM_003392.7(WNT5A):c.*1428TA[6]	rs374828022
NM_003392.7(WNT5A):c.*1428TA[8]	rs374828022
NM_003392.7(WNT5A):c.*1444TA[5]	rs886058741
NM_003392.7(WNT5A):c.1952_1953del	rs78756487
NM_003392.7(WNT5A):c.1952_1953dup	rs78756487
NM_003392.7(WNT5A):c.*1953dup	rs78756487
NM_003392.7(WNT5A):c.2711_2713del	rs760058727
NM_003392.7(WNT5A):c.2728_2730del	rs886058738
NM_003392.7(WNT5A):c.*2728del	rs142609857
NM_003392.7(WNT5A):c.*2731dup	rs886058737
NM_003392.7(WNT5A):c.*3932CT[3]	rs886058733

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