List of variants in gene PMS2 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: 17

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HGVS	dbSNP	gnomAD frequency
NM_000535.7(PMS2):c.1488C>T (p.His496=)	rs1805320	0.02307
NM_000535.7(PMS2):c.1866G>A (p.Met622Ile)	rs1805324	0.01651
NM_000535.7(PMS2):c.1557T>C (p.Tyr519=)	rs6972869	0.01065
NM_000535.7(PMS2):c.1569C>G (p.Ser523=)	rs141458772	0.00560
NM_000535.7(PMS2):c.1266G>A (p.Glu422=)	rs138049175	0.00348
NM_000535.7(PMS2):c.383C>T (p.Ser128Leu)	rs116373169	0.00177
NM_000535.7(PMS2):c.2340C>T (p.Pro780=)	rs142230276	0.00117
NM_000535.7(PMS2):c.1560G>A (p.Ala520=)	rs201167814	0.00039
NM_000535.7(PMS2):c.953A>G (p.Tyr318Cys)	rs139438201	0.00022
NM_000535.7(PMS2):c.1467G>A (p.Glu489=)	rs542522853	0.00015
NM_000535.7(PMS2):c.477G>A (p.Val159=)	rs147701251	0.00006
NM_000535.7(PMS2):c.1197G>A (p.Lys399=)	rs757730609	0.00004
NM_000535.7(PMS2):c.1435C>G (p.His479Asp)	rs376344586	0.00002
NM_000535.7(PMS2):c.1753C>A (p.Leu585Ile)	rs63750947	0.00001
NM_000535.7(PMS2):c.187G>A (p.Val63Met)	rs772216832	0.00001
NM_000535.7(PMS2):c.1688G>T (p.Arg563Leu)	rs63750668
NM_000535.7(PMS2):c.830C>A (p.Thr277Lys)	rs1805322

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