List of variants in gene MSH6 reported as uncertain significance by GeneKor MSA

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_000179.3(MSH6):c.2398G>C (p.Val800Leu)	rs61748083	0.00014
NM_000179.3(MSH6):c.3727A>T (p.Thr1243Ser)	rs147453999	0.00009
NM_000179.3(MSH6):c.1814C>G (p.Thr605Ser)	rs587781616	0.00006
NM_000179.3(MSH6):c.1402C>T (p.Arg468Cys)	rs369456858	0.00004
NM_000179.3(MSH6):c.1025C>G (p.Ala342Gly)	rs753617680	0.00003
NM_000179.3(MSH6):c.4002-4T>C	rs370428032	0.00001
NM_000179.3(MSH6):c.1615CTT[1] (p.Leu540del)	rs1064793600
NM_000179.3(MSH6):c.2622C>T (p.Ile874=)	rs1200093419
NM_000179.3(MSH6):c.2806G>C (p.Asp936His)	rs876659904
NM_000179.3(MSH6):c.2975A>G (p.Glu992Gly)	rs876660688
NM_000179.3(MSH6):c.3349T>C (p.Cys1117Arg)	rs786202829
NM_000179.3(MSH6):c.3758T>A (p.Val1253Glu)	rs202066386
NM_000179.3(MSH6):c.3832C>G (p.Pro1278Ala)	rs587782109
NM_000179.3(MSH6):c.893G>A (p.Arg298Gln)	rs765237563
NM_000179.3(MSH6):c.95G>A (p.Gly32Asp)	rs771426932

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