List of variants in gene combination DHFR, MSH3 reported as benign for hematologic disorder

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_000791.4(DHFR):c.-473T>C	rs1650697	0.80068
NM_000791.4(DHFR):c.-400A>G	rs2405875	0.02618
NM_000791.4(DHFR):c.-416C>G	rs2001675	0.00949
NM_000791.4(DHFR):c.-259C>T	rs6151597	0.00658
NM_000791.4(DHFR):c.-406CGCTGCAGC[1]	rs758595508
NM_000791.4(DHFR):c.-418GGCCGCTGC[1]	rs758960105
NM_000791.4(DHFR):c.-437GGGGCGCTG[3]	rs60484572
NM_000791.4(DHFR):c.-442_-434del	rs3045983
NM_002439.5(MSH3):c.162_179del (p.Ala57_Ala62del)	rs201874762

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