List of variants in gene MARS2 reported as benign for not provided

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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_138395.4(MARS2):c.166_168dup	rs3832092	0.51686
NM_138395.4(MARS2):c.471C>T (p.Arg157=)	rs35544931	0.01792
NM_138395.4(MARS2):c.24C>G (p.Arg8=)	rs116491566	0.00735
NM_138395.4(MARS2):c.606A>G (p.Pro202=)	rs34908171	0.00581
NM_138395.4(MARS2):c.748C>T (p.Leu250=)	rs61749522	0.00435
NM_138395.4(MARS2):c.1580T>C (p.Val527Ala)	rs141544058	0.00387
NM_138395.4(MARS2):c.1615C>T (p.Leu539=)	rs114183325	0.00271
NM_138395.4(MARS2):c.801G>C (p.Pro267=)	rs144114997	0.00027
NM_138395.4(MARS2):c.697A>G (p.Ile233Val)	rs150082953	0.00022
NM_138395.4(MARS2):c.60C>T (p.Leu20=)	rs201033319	0.00011
NM_138395.4(MARS2):c.124G>A (p.Asp42Asn)	rs200490327	0.00006
NM_138395.4(MARS2):c.1297C>G (p.Pro433Ala)	rs564555725	0.00005
NM_138395.4(MARS2):c.1173G>C (p.Val391=)	rs117988876	0.00003

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