List of variants in gene LRSAM1 reported as uncertain significance by Genesis Genome Database

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_001005373.4(LRSAM1):c.1142G>A (p.Arg381Gln)	rs145877456	0.00002
NM_001005373.4(LRSAM1):c.119del (p.Glu40fs)	rs1588090984
NM_001005373.4(LRSAM1):c.1775A>C (p.His592Pro)	rs1039132247
NM_001005373.4(LRSAM1):c.2005G>T (p.Glu669Ter)	rs1588143112
NM_001005373.4(LRSAM1):c.2047-3C>T	rs1588144581
NM_001005373.4(LRSAM1):c.2134_2145del (p.Asp712_Gln715del)	rs1588144737
NM_001005373.4(LRSAM1):c.86G>C (p.Gly29Ala)	rs142846298

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