List of variants in gene combination LOC114827851, MYH6 reported by PreventionGenetics, part of Exact Sciences

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 19

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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.330G>A (p.Ala110=)	rs77679218	0.00490
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.408C>T (p.Ala136=)	rs140732380	0.00024
NM_002471.4(MYH6):c.-8G>A	rs28730779	0.00009
NM_002471.4(MYH6):c.182C>T (p.Ala61Val)	rs730880148	0.00001
NM_002471.4(MYH6):c.120C>T (p.Pro40=)
NM_002471.4(MYH6):c.341T>C (p.Ile114Thr)
NM_002471.4(MYH6):c.353C>A (p.Ser118Ter)
NM_002471.4(MYH6):c.427C>A (p.Arg143=)	rs2277473
NM_002471.4(MYH6):c.43T>A (p.Tyr15Asn)
NM_002471.4(MYH6):c.475G>A (p.Asp159Asn)
NM_002471.4(MYH6):c.50G>T (p.Arg17Leu)	rs746646172
NM_002471.4(MYH6):c.546G>A (p.Ala182=)	rs150015506
NM_002471.4(MYH6):c.70C>A (p.Leu24Ile)	rs573489857

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