List of variants in gene MSH6 reported as likely benign by True Health Diagnostics

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.1164C>T (p.His388=)	rs55708305	0.01384
NM_000179.3(MSH6):c.2272C>T (p.Leu758=)	rs56371757	0.01363
NM_000179.3(MSH6):c.3306T>A (p.Thr1102=)	rs2020910	0.00869
NM_000179.3(MSH6):c.663A>C (p.Glu221Asp)	rs41557217	0.00064
NM_000179.3(MSH6):c.3960A>G (p.Ala1320=)	rs373425206	0.00042
NM_000179.3(MSH6):c.1449G>T (p.Val483=)	rs35590297	0.00037
NM_000179.3(MSH6):c.2940A>G (p.Glu980=)	rs730881818	0.00001
NM_000179.3(MSH6):c.3246G>A (p.Pro1082=)	rs3136351
NM_000179.3(MSH6):c.3246G>T (p.Pro1082=)	rs3136351
NM_000179.3(MSH6):c.4001+2TAAC[2]	rs267608132
NM_000179.3(MSH6):c.603G>A (p.Glu201=)	rs587779314

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