List of variants in gene MYBPC3 reported as likely benign by Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen

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: 25

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HGVS	dbSNP	gnomAD frequency
NM_000256.3(MYBPC3):c.1458-17C>T	rs3729945	0.00203
NM_000256.3(MYBPC3):c.1608T>A (p.Ala536=)	rs200224422	0.00176
NM_000256.3(MYBPC3):c.2905+35A>G	rs11570107	0.00175
NM_000256.3(MYBPC3):c.2497G>A (p.Ala833Thr)	rs199865688	0.00122
NM_000256.3(MYBPC3):c.3413G>A (p.Arg1138His)	rs187705120	0.00106
NM_000256.3(MYBPC3):c.2914C>T (p.Arg972Trp)	rs193922382	0.00096
NM_000256.3(MYBPC3):c.3392T>C (p.Ile1131Thr)	rs370890951	0.00076
NM_000256.3(MYBPC3):c.646G>A (p.Ala216Thr)	rs201098973	0.00076
NM_000256.3(MYBPC3):c.471C>T (p.Phe157=)	rs150291001	0.00034
NM_000256.3(MYBPC3):c.961G>A (p.Val321Met)	rs200119454	0.00025
NM_000256.3(MYBPC3):c.184A>C (p.Thr62Pro)	rs377225516	0.00024
NM_000256.3(MYBPC3):c.506-17C>T	rs561595897	0.00016
NM_000256.3(MYBPC3):c.531C>T (p.Arg177=)	rs368035400	0.00012
NM_000256.3(MYBPC3):c.1467C>T (p.Asp489=)	rs35690719	0.00011
NM_000256.3(MYBPC3):c.3107G>A (p.Arg1036His)	rs374255381	0.00007
NM_000256.3(MYBPC3):c.3573G>A (p.Ser1191=)	rs371488508	0.00004
NM_000256.3(MYBPC3):c.540C>T (p.Gly180=)	rs371842442	0.00004
NM_000256.3(MYBPC3):c.1790+7G>A	rs374852831	0.00003
NM_000256.3(MYBPC3):c.654+18G>A	rs758836172	0.00003
NM_000256.3(MYBPC3):c.1593G>A (p.Gly531=)	rs727503199	0.00002
NM_000256.3(MYBPC3):c.2112C>T (p.Asp704=)	rs547477069	0.00002
NM_000256.3(MYBPC3):c.705C>T (p.Gly235=)	rs767913494	0.00001
NM_000256.3(MYBPC3):c.1008C>T (p.Ile336=)	rs397515880
NM_000256.3(MYBPC3):c.1311G>C (p.Val437=)	rs1060504240
NM_000256.3(MYBPC3):c.3471C>T (p.Pro1157=)	rs962554743

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