List of variants in gene combination CDCA7L, DNAH11 reported by PreventionGenetics, part of Exact Sciences

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_001277115.2(DNAH11):c.13502A>G (p.Lys4501Arg)	rs77448980	0.06056
NM_001277115.2(DNAH11):c.13547C>T (p.Ala4516Val)	rs72658840	0.02832
NM_018719.5(CDCA7L):c.*1052G>A	rs72658841	0.01754
NM_001277115.2(DNAH11):c.13495G>A (p.Glu4499Lys)	rs143362381	0.00403
NM_001277115.2(DNAH11):c.13406G>A (p.Arg4469Lys)	rs183031009	0.00120
NM_001277115.2(DNAH11):c.13548G>A (p.Ala4516=)	rs147454485	0.00080
NM_001277115.2(DNAH11):c.13305C>T (p.Gly4435=)	rs150682314	0.00029
NM_001277115.2(DNAH11):c.13399G>A (p.Val4467Met)	rs200609513	0.00020
NM_001277115.2(DNAH11):c.13499A>G (p.Glu4500Gly)
NM_001277115.2(DNAH11):c.13542A>G (p.Leu4514=)

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