List of variants in gene MLYCD reported as likely benign for not specified

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_012213.3(MLYCD):c.408C>G (p.Arg136=)	rs183593320	0.00108
NM_012213.3(MLYCD):c.375C>G (p.Ala125=)	rs375657338	0.00096
NM_012213.3(MLYCD):c.1098C>T (p.Ile366=)	rs199549095	0.00048
NM_012213.3(MLYCD):c.1074G>A (p.Ser358=)	rs377161125	0.00043
NM_012213.3(MLYCD):c.1383G>A (p.Thr461=)	rs375344095	0.00027
NM_012213.3(MLYCD):c.393C>T (p.Tyr131=)	rs560831102	0.00015
NM_012213.3(MLYCD):c.1146C>T (p.Ser382=)	rs373273203	0.00010
NM_012213.3(MLYCD):c.1191G>A (p.Pro397=)	rs753701525	0.00001
NM_012213.3(MLYCD):c.529-20A>G	rs1555538216

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