List of variants in gene APC reported as uncertain significance by Eurofins NTD LLC (GA)

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_000038.6(APC):c.2232T>G (p.Ser744=)	rs145751759	0.00032
NM_000038.6(APC):c.6724A>G (p.Ser2242Gly)	rs201375478	0.00008
NM_000038.6(APC):c.1005A>G (p.Leu335=)	rs3797704	0.00006
NM_000038.6(APC):c.2250A>T (p.Pro750=)	rs376526724	0.00006
NM_000038.6(APC):c.4478C>T (p.Thr1493Met)	rs374892194	0.00006
NM_000038.6(APC):c.5528C>T (p.Pro1843Leu)	rs368080169	0.00004
NM_000038.6(APC):c.6131G>A (p.Ser2044Asn)	rs375743017	0.00003
NM_000038.6(APC):c.5363G>A (p.Arg1788His)	rs201472075	0.00002
NM_000038.6(APC):c.3760A>G (p.Ile1254Val)	rs769504783	0.00001
NM_000038.6(APC):c.4212C>T (p.Ser1404=)	rs144655979

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