List of variants in gene combination LOC114827851, MYH6 reported as benign for hypertrophic cardiomyopathy 14

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 16

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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.622G>A (p.Asp208Asn)	rs142027794	0.00415
NM_002471.4(MYH6):c.210T>C (p.Thr70=)	rs147397431	0.00041
NM_002471.4(MYH6):c.492C>T (p.Tyr164=)	rs201380776	0.00041
NM_002471.4(MYH6):c.642+16C>T	rs547762012	0.00025
NM_002471.4(MYH6):c.427C>A (p.Arg143=)	rs2277473
NM_002471.4(MYH6):c.502+14C>A
NM_002471.4(MYH6):c.503-10_503-8del
NM_002471.4(MYH6):c.70C>A (p.Leu24Ile)	rs573489857

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