List of variants in gene combination DHFR, MSH3 reported as benign by GeneDx

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_000791.4(DHFR):c.-473T>C	rs1650697	0.80068
NM_002439.5(MSH3):c.-35A>G	rs1105524	0.63625
NM_002439.5(MSH3):c.-50C>T	rs2250063	0.25491
NC_000005.10:g.80654584C>T	rs10168	0.25445
NC_000005.10:g.80654344_80654345insTGGCGCGTCCCGCCCAGGT	rs70991108
NC_000005.10:g.80654576del	rs151182735
NM_000791.4(DHFR):c.-417_-416insGCGCTGCGGCCGCTGCGG	rs758718643
NM_000791.4(DHFR):c.-418GGCCGCTGC[1]	rs758960105
NM_000791.4(DHFR):c.-425_-417dup	rs1554066076
NM_000791.4(DHFR):c.-437GGGGCGCTG[1]	rs60484572
NM_000791.4(DHFR):c.-442_-434del	rs3045983
NM_002439.5(MSH3):c.-39C>T	rs1105525
NM_002439.5(MSH3):c.162_179del (p.Ala57_Ala62del)	rs201874762

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