List of variants in gene ANTXR1 reported as benign for GAPO syndrome

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_032208.3(ANTXR1):c.703+78T>G	rs4241348	0.93937
NM_032208.3(ANTXR1):c.643-66G>A	rs4854546	0.92047
NM_032208.3(ANTXR1):c.1185+16C>A	rs6749826	0.45542
NM_032208.3(ANTXR1):c.379-69T>C	rs13030844	0.41577
NM_032208.3(ANTXR1):c.873-76T>A	rs11126217	0.37565
NM_032208.3(ANTXR1):c.802+46A>G	rs6710260	0.33620
NM_032208.3(ANTXR1):c.642+99T>C	rs7424907	0.11724
NM_032208.3(ANTXR1):c.492+10G>A	rs10202939	0.11594
NM_032208.3(ANTXR1):c.413-61G>A	rs548701918	0.11514
NM_032208.3(ANTXR1):c.413-65_413-63del	rs67110959	0.11512
NM_032208.3(ANTXR1):c.413-67G>C	rs57008189	0.11511
NM_032208.3(ANTXR1):c.153-42G>A	rs4366940	0.05922
NM_032208.3(ANTXR1):c.224+81A>G	rs4527236	0.04443
NM_032208.3(ANTXR1):c.152+89G>C	rs116312139	0.03682
NM_032208.3(ANTXR1):c.379-32T>G	rs77557115	0.03102
NM_032208.3(ANTXR1):c.1434+45_1434+46insTCAC	rs57847359
NM_032208.3(ANTXR1):c.1434+49T>C	rs7584057

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