List of variants in gene LRSAM1 reported as benign by Illumina Laboratory Services, Illumina

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_001005373.4(LRSAM1):c.952A>G (p.Asn318Asp)	rs1539567	0.75123
NM_001005373.4(LRSAM1):c.1912+5A>C	rs2248822	0.74956
NM_001005373.4(LRSAM1):c.249C>T (p.Ile83=)	rs2243906	0.61095
NM_001005373.4(LRSAM1):c.904-9C>T	rs1539568	0.43695
NM_001005373.4(LRSAM1):c.548C>T (p.Ser183Leu)	rs75690855	0.03450
NM_001005373.4(LRSAM1):c.1830+6C>T	rs75171318	0.01846
NM_001005373.4(LRSAM1):c.1368G>A (p.Ala456=)	rs34426300	0.00573
NM_001005373.4(LRSAM1):c.1044-9T>C	rs59501881	0.00523
NM_001005373.4(LRSAM1):c.1975G>A (p.Val659Met)	rs140786088	0.00342
NM_001005373.4(LRSAM1):c.965A>G (p.Gln322Arg)	rs56380300	0.00328
NM_001005373.4(LRSAM1):c.*57G>A	rs549468112	0.00273
NM_001005373.4(LRSAM1):c.268G>A (p.Asp90Asn)	rs117692127	0.00133
NM_001005373.4(LRSAM1):c.619+13C>T	rs148704769	0.00005

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