List of variants reported as likely benign for autosomal recessive limb-girdle muscular dystrophy type 2H by Fulgent Genetics, Fulgent Genetics

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Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_012210.4(TRIM32):c.1223G>A (p.Arg408His)	rs183136193	0.00006
NM_012210.4(TRIM32):c.1275T>C (p.Asp425=)	rs150813870	0.00005
NM_012210.4(TRIM32):c.404C>T (p.Thr135Ile)	rs141953092	0.00005
NM_012210.4(TRIM32):c.1609C>T (p.Leu537=)	rs139275673	0.00004
NM_012210.4(TRIM32):c.1623G>A (p.Gln541=)	rs201083322	0.00004
NM_012210.4(TRIM32):c.1728C>T (p.Arg576=)	rs774825642	0.00002
NM_012210.4(TRIM32):c.474A>G (p.Glu158=)	rs955416816	0.00001
NM_012210.4(TRIM32):c.216C>T (p.Ser72=)	rs1860954629
NM_012210.4(TRIM32):c.378A>G (p.Ala126=)	rs1860970214
NM_012210.4(TRIM32):c.939G>T (p.Ala313=)	rs375442860

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