List of variants in gene MSH6 reported as likely benign by Fulgent Genetics, Fulgent Genetics

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_000179.3(MSH6):c.3439-16C>T	rs192614006	0.00237
NM_000179.3(MSH6):c.1526T>C (p.Val509Ala)	rs63751005	0.00067
NM_000179.3(MSH6):c.1508C>G (p.Ser503Cys)	rs63750897	0.00059
NM_000179.3(MSH6):c.3172+20T>C	rs3136335	0.00009
NM_000179.3(MSH6):c.660A>C (p.Glu220Asp)	rs1800938	0.00009
NM_000179.3(MSH6):c.3557-17A>T	rs542542093	0.00004
NM_000179.3(MSH6):c.3801+14G>T	rs755626529	0.00002
NM_000179.3(MSH6):c.3228C>T (p.Arg1076=)	rs786203698
NM_000179.3(MSH6):c.3557-4dup	rs267608102
NM_000179.3(MSH6):c.4001+2TAAC[2]	rs267608132
NM_000179.3(MSH6):c.4001+2TAAC[4]	rs267608132

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