List of variants in gene MMAA studied for MMAA-related condition

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_172250.3(MMAA):c.966A>G (p.Pro322=)	rs150692463	0.00073
NM_172250.3(MMAA):c.57A>G (p.Ala19=)	rs143211378	0.00035
NM_172250.3(MMAA):c.433C>T (p.Arg145Ter)	rs104893851	0.00017
NM_172250.3(MMAA):c.729C>T (p.Thr243=)	rs138111772	0.00014
NM_172250.3(MMAA):c.-4G>A	rs374109118	0.00004
NM_172250.3(MMAA):c.378A>G (p.Val126=)	rs750237065	0.00004
NM_172250.3(MMAA):c.387C>A (p.Tyr129Ter)	rs796051992	0.00003
NM_172250.3(MMAA):c.585C>T (p.Thr195=)	rs571797666	0.00002
NM_172250.3(MMAA):c.833G>A (p.Gly278Asp)	rs761964238	0.00001
NM_172250.3(MMAA):c.639del (p.Arg214fs)	rs2126622813
NM_172250.3(MMAA):c.915A>G (p.Glu305=)

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