List of variants in gene combination LOC114827851, MYH6 reported as benign for not specified

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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: 18

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HGVS	dbSNP	gnomAD frequency
NM_002471.4(MYH6):c.411G>A (p.Glu137=)	rs2277474	0.22054
NM_002471.4(MYH6):c.393G>A (p.Leu131=)	rs17277970	0.06973
NM_002471.4(MYH6):c.166G>A (p.Gly56Arg)	rs28711516	0.06950
NM_002471.4(MYH6):c.201+16C>T	rs7147244	0.06154
NM_002471.4(MYH6):c.399G>A (p.Val133=)	rs78891557	0.01343
NM_002471.4(MYH6):c.330G>A (p.Ala110=)	rs77679218	0.00490
NM_002471.4(MYH6):c.36G>A (p.Ala12=)	rs141014719	0.00487
NM_002471.4(MYH6):c.86G>A (p.Arg29Gln)	rs150574114	0.00455
NM_002471.4(MYH6):c.-5C>A	rs183611755	0.00438
NM_002471.4(MYH6):c.622G>A (p.Asp208Asn)	rs142027794	0.00415
NM_002471.4(MYH6):c.531-19T>A	rs374174532	0.00045
NM_002471.4(MYH6):c.210T>C (p.Thr70=)	rs147397431	0.00041
NM_002471.4(MYH6):c.642+16C>T	rs547762012	0.00025
NM_002471.4(MYH6):c.420C>T (p.Ala140=)	rs145023897	0.00010
NM_002471.4(MYH6):c.-8G>A	rs28730779	0.00009
NM_002471.4(MYH6):c.252C>T (p.Phe84=)	rs397516757	0.00001
NM_002471.4(MYH6):c.427C>A (p.Arg143=)	rs2277473
NM_002471.4(MYH6):c.70C>A (p.Leu24Ile)	rs573489857

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