List of variants reported as likely benign for Atelosteogenesis type II by Illumina Laboratory Services, Illumina

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Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_000112.4(SLC26A2):c.*4799G>A	rs72832119	0.01211
NM_000112.4(SLC26A2):c.*2873C>T	rs114919633	0.00970
NM_000112.4(SLC26A2):c.-183G>C	rs540241474	0.00338
NM_000112.4(SLC26A2):c.*3507T>A	rs180966130	0.00309
NM_000112.4(SLC26A2):c.*205G>A	rs115383424	0.00280
NM_000112.4(SLC26A2):c.*443T>C	rs115977282	0.00246
NM_000112.4(SLC26A2):c.987T>C (p.Leu329=)	rs116302615	0.00246
NM_000112.4(SLC26A2):c.*4659G>T	rs143908264	0.00169
NM_000112.4(SLC26A2):c.*1970G>T	rs147208348	0.00148
NM_000112.4(SLC26A2):c.1512G>A (p.Met504Ile)	rs76668544	0.00022
NM_000112.4(SLC26A2):c.*3918C>T	rs192457706	0.00003
NM_000112.4(SLC26A2):c.*2476T>C	rs570682108
NM_000112.4(SLC26A2):c.*4419A>C	rs140200789

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