List of variants in gene combination MHRT, MYH7 reported as benign

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: 36

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HGVS	dbSNP	gnomAD frequency
NM_000257.4(MYH7):c.4644+80C>T	rs3729828	0.43652
NM_000257.4(MYH7):c.4644+190C>T	rs3729829	0.43603
NM_000257.4(MYH7):c.4645-173C>T	rs7140721	0.43561
NM_000257.4(MYH7):c.4520-63G>A	rs3729825	0.19597
NM_000257.4(MYH7):c.4353+42G>A	rs3729822	0.06369
NM_000257.4(MYH7):c.4644+57C>G	rs3729827	0.02808
NM_000257.4(MYH7):c.4353+17G>A	rs45581933	0.01445
NM_000257.4(MYH7):c.4472C>G (p.Ser1491Cys)	rs3729823	0.00861
NM_000257.4(MYH7):c.4566T>C (p.Thr1522=)	rs2754155	0.00831
NM_000257.4(MYH7):c.4520-25C>T	rs45503601	0.00787
NM_000257.4(MYH7):c.4644+24G>T	rs3729826	0.00312
NM_000257.4(MYH7):c.4452C>T (p.Leu1484=)	rs61737803	0.00275
NM_000257.4(MYH7):c.4353+10G>A	rs202205780	0.00274
NM_000257.4(MYH7):c.4377G>T (p.Lys1459Asn)	rs201307101	0.00024
NM_000257.4(MYH7):c.4354-6G>A	rs368078397	0.00009
NM_000257.4(MYH7):c.4618C>T (p.Leu1540=)	rs368734580	0.00007
NM_000257.4(MYH7):c.4283T>C (p.Leu1428Ser)	rs727503244	0.00006
NM_000257.4(MYH7):c.4290G>T (p.Val1430=)	rs372476972	0.00005
NM_000257.4(MYH7):c.4410G>A (p.Ser1470=)	rs578166720	0.00004
NM_000257.4(MYH7):c.4520-15G>A	rs200886528	0.00004
NM_000257.4(MYH7):c.4500G>A (p.Arg1500=)	rs199995198	0.00002
NM_000257.4(MYH7):c.4557C>T (p.Ser1519=)	rs150552664	0.00002
NM_000257.4(MYH7):c.4641C>T (p.Ala1547=)	rs376854724	0.00002
NM_000257.4(MYH7):c.4326G>A (p.Leu1442=)	rs727503243	0.00001
NM_000257.4(MYH7):c.4353+20C>T	rs199912646	0.00001
NM_000257.4(MYH7):c.4353+13T>G	rs587781084
NM_000257.4(MYH7):c.4353+18del	rs2138646248
NM_000257.4(MYH7):c.4353+9T>G	rs2138646292
NM_000257.4(MYH7):c.4354-7C>T	rs370093487
NM_000257.4(MYH7):c.4399C>G (p.Leu1467Val)	rs397516214
NM_000257.4(MYH7):c.4519+9G>C	rs2138645065
NM_000257.4(MYH7):c.4520-38C>G	rs1361469373
NM_000257.4(MYH7):c.4520-42A>T	rs2138644761
NM_000257.4(MYH7):c.4644+1del	rs2138644180
NM_000257.4(MYH7):c.4644+2del	rs2138644167
NM_000257.4(MYH7):c.4645-196C>T	rs76614781

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