List of variants in gene MMAB 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: 26

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HGVS	dbSNP	gnomAD frequency
NM_052845.4(MMAB):c.716T>A (p.Met239Lys)	rs9593	0.57816
NM_052845.4(MMAB):c.*1230G>T	rs11067231	0.57792
NM_052845.4(MMAB):c.*857G>C	rs877710	0.57567
NM_052845.4(MMAB):c.*2701G>C	rs2241201	0.33323
NM_052845.4(MMAB):c.*3148G>A	rs11067227	0.24433
NM_052845.4(MMAB):c.*625G>C	rs11067233	0.24420
NM_052845.4(MMAB):c.*891C>A	rs877709	0.24416
NM_052845.4(MMAB):c.*1535G>A	rs34921355	0.17160
NM_052845.4(MMAB):c.*2835T>C	rs12817689	0.17090
NM_052845.4(MMAB):c.*2684G>C	rs35145546	0.16925
NM_052845.4(MMAB):c.*1467C>T	rs1061440	0.10807
NM_052845.4(MMAB):c.*192T>C	rs8228	0.10802
NM_052845.4(MMAB):c.*1952T>C	rs61940463	0.10789
NM_052845.4(MMAB):c.*1810G>A	rs73414076	0.10702
NM_052845.4(MMAB):c.*721T>G	rs11831226	0.09002
NM_052845.4(MMAB):c.*378T>A	rs66497319	0.08528
NM_052845.4(MMAB):c.*656C>A	rs11067232	0.06631
NM_052845.4(MMAB):c.*1729A>C	rs559163901	0.06120
NM_052845.4(MMAB):c.*376T>A	rs527861371	0.05729
NM_052845.4(MMAB):c.*1005A>G	rs67432283	0.05428
NM_052845.4(MMAB):c.*1657G>A	rs111869218	0.05172
NM_052845.4(MMAB):c.*3178C>A	rs73414071	0.02490
NM_052845.4(MMAB):c.*2628C>T	rs73414074	0.02477
NM_052845.4(MMAB):c.*564G>C	rs56760240	0.02466
NM_052845.4(MMAB):c.*374T>A	rs549601416	0.02435
NM_052845.4(MMAB):c.*380A>T	rs74967596	0.01505

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