List of variants in gene MMAA reported as benign by Illumina Laboratory Services, Illumina

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_172250.3(MMAA):c.*2608T>C	rs7699187	0.51441
NM_172250.3(MMAA):c.*2768A>T	rs7699166	0.51403
NM_172250.3(MMAA):c.*2866A>G	rs17020500	0.22820
NM_172250.3(MMAA):c.747G>A (p.Ser249=)	rs11721553	0.07844
NM_172250.3(MMAA):c.*3621G>A	rs55770806	0.07335
NM_172250.3(MMAA):c.-56A>G	rs4835011	0.06388
NM_172250.3(MMAA):c.1089G>C (p.Gln363His)	rs2270655	0.04892
NM_172250.3(MMAA):c.*2142T>C	rs72723824	0.03954
NM_172250.3(MMAA):c.*2658G>A	rs72723825	0.03953
NM_172250.3(MMAA):c.*306T>A	rs74409983	0.03738
NM_172250.3(MMAA):c.*2372T>A	rs74719174	0.02233
NM_172250.3(MMAA):c.*434C>T	rs72950841	0.01492
NM_172250.3(MMAA):c.*3824C>A	rs72950842	0.01396
NM_172250.3(MMAA):c.*4336A>G	rs138752110	0.01347
NM_172250.3(MMAA):c.*1782A>G	rs114134771	0.01301
NM_172250.3(MMAA):c.138T>C (p.Ser46=)	rs34702224	0.01204

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