List of variants in gene MYH3 reported as likely benign for Distal arthrogryposis type 2B1

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_002470.4(MYH3):c.4356+11C>T	rs150348272	0.00505
NM_002470.4(MYH3):c.690C>G (p.Ala230=)	rs147148934	0.00421
NM_002470.4(MYH3):c.4172+9C>T	rs116028239	0.00364
NM_002470.4(MYH3):c.4910C>T (p.Ala1637Val)	rs34165480	0.00311
NM_002470.4(MYH3):c.2926-8C>T	rs188588330	0.00296
NM_002470.4(MYH3):c.4098T>C (p.Asn1366=)	rs138944611	0.00291
NM_002470.4(MYH3):c.3594G>A (p.Ala1198=)	rs139978727	0.00252
NM_002470.4(MYH3):c.5109G>A (p.Ala1703=)	rs114770362	0.00250
NM_002470.4(MYH3):c.1566C>A (p.Ile522=)	rs146873206	0.00236
NM_002470.4(MYH3):c.1411T>C (p.Tyr471His)	rs115742228	0.00227
NM_002470.4(MYH3):c.2289+4A>G	rs111835858	0.00218
NM_002470.4(MYH3):c.-63G>A	rs141754213	0.00209
NM_002470.4(MYH3):c.5067G>T (p.Leu1689=)	rs112858125	0.00205
NM_002470.4(MYH3):c.1932C>T (p.Ser644=)	rs115612890	0.00194
NM_002470.4(MYH3):c.3078C>T (p.Ser1026=)	rs146309217	0.00158
NM_002470.4(MYH3):c.252G>A (p.Lys84=)	rs147410236	0.00156
NM_002470.4(MYH3):c.5390G>A (p.Arg1797His)	rs138194008	0.00152
NM_002470.4(MYH3):c.3479C>T (p.Thr1160Met)	rs145080512	0.00137
NM_002470.4(MYH3):c.2883C>A (p.Thr961=)	rs144338240	0.00096
NM_002470.4(MYH3):c.4082C>T (p.Ala1361Val)	rs140218185	0.00096
NM_002470.4(MYH3):c.642+10G>A	rs183463746	0.00092
NM_002470.4(MYH3):c.736-6A>G	rs372079063	0.00067
NM_002470.4(MYH3):c.3612T>C (p.Leu1204=)	rs146773743	0.00063
NM_002470.4(MYH3):c.3731C>T (p.Ala1244Val)	rs140074626	0.00054
NM_002470.4(MYH3):c.4647+6T>G	rs375163919	0.00054
NM_002470.4(MYH3):c.1521C>T (p.Ile507=)	rs140685610	0.00029
NM_002470.4(MYH3):c.412G>A (p.Glu138Lys)	rs191837780	0.00029
NM_002470.4(MYH3):c.5274G>A (p.Lys1758=)	rs377092561	0.00028
NM_002470.4(MYH3):c.3389G>A (p.Arg1130His)	rs184919169	0.00022
NM_002470.4(MYH3):c.5797-12C>G	rs374799651	0.00018
NM_002470.4(MYH3):c.5074A>G (p.Thr1692Ala)	rs140180067	0.00010
NM_002470.4(MYH3):c.3039T>C (p.Ala1013=)	rs142131471	0.00006
NM_002470.4(MYH3):c.3462G>A (p.Ala1154=)	rs201553125	0.00006
NM_002470.4(MYH3):c.4941C>T (p.Val1647=)	rs143855213	0.00004
NM_002470.4(MYH3):c.3509C>A (p.Ala1170Glu)	rs373367650
NM_002470.4(MYH3):c.4451A>G (p.Lys1484Arg)	rs537656234

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