List of variants in gene LRSAM1 reported as uncertain significance by Molecular Genetics Laboratory, London Health Sciences Centre

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: 22

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HGVS	dbSNP	gnomAD frequency
NM_001005373.4(LRSAM1):c.814C>T (p.Arg272Trp)	rs149456922	0.00063
NM_001005373.4(LRSAM1):c.586G>A (p.Gly196Ser)	rs148059394	0.00045
NM_001005373.4(LRSAM1):c.1406G>A (p.Arg469Gln)	rs369439346	0.00031
NM_001005373.4(LRSAM1):c.94G>A (p.Asp32Asn)	rs150784835	0.00017
NM_001005373.4(LRSAM1):c.1601C>T (p.Thr534Met)	rs141542114	0.00015
NM_001005373.4(LRSAM1):c.1781G>A (p.Arg594His)	rs537838691	0.00004
NM_001005373.4(LRSAM1):c.1837G>A (p.Val613Ile)	rs746831085	0.00004
NM_001005373.4(LRSAM1):c.392C>T (p.Thr131Ile)	rs772202137	0.00004
NM_001005373.4(LRSAM1):c.685G>A (p.Glu229Lys)	rs563259179	0.00004
NM_001005373.4(LRSAM1):c.992C>T (p.Thr331Met)	rs775480266	0.00004
NM_001005373.4(LRSAM1):c.1714C>T (p.Arg572Cys)	rs1359751742	0.00002
NM_001005373.4(LRSAM1):c.904-4del	rs757987823	0.00002
NM_001005373.4(LRSAM1):c.1198C>T (p.Arg400Trp)	rs749575647	0.00001
NM_001005373.4(LRSAM1):c.1619G>T (p.Ser540Ile)	rs1400819662	0.00001
NM_001005373.4(LRSAM1):c.362G>A (p.Arg121His)	rs143910539	0.00001
NM_001005373.4(LRSAM1):c.604C>G (p.Gln202Glu)	rs746274685	0.00001
NM_001005373.4(LRSAM1):c.1261A>G (p.Met421Val)	rs1835780785
NM_001005373.4(LRSAM1):c.1419C>A (p.Ser473Arg)	rs1345645228
NM_001005373.4(LRSAM1):c.1753C>G (p.His585Asp)	rs1183629673
NM_001005373.4(LRSAM1):c.1936G>T (p.Val646Phe)	rs748358043
NM_001005373.4(LRSAM1):c.2087G>A (p.Cys696Tyr)	rs1588144651
NM_001005373.4(LRSAM1):c.253-9C>A	rs199925705

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