List of variants reported for not specified by Fulgent Genetics, Fulgent Genetics

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		ClinVar version:

Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_006393.3(NEBL):c.604G>A (p.Gly202Arg)	rs137973321	0.00210
NM_000940.3(PON3):c.94C>T (p.Arg32Ter)	rs147006695	0.00195
NM_032531.4(KIRREL3):c.908T>C (p.Val303Ala)	rs201725914	0.00056
NM_000940.3(PON3):c.496G>A (p.Val166Met)	rs201544566	0.00036
NM_012301.4(MAGI2):c.2131C>A (p.Pro711Thr)	rs144078604	0.00031
NM_006393.3(NEBL):c.2417C>T (p.Thr806Ile)	rs200705273	0.00020
NM_003803.4(MYOM1):c.3665A>G (p.Tyr1222Cys)	rs748819463	0.00008
NM_005379.4(MYO1A):c.1678C>G (p.Pro560Ala)	rs140586750	0.00004
NM_001128205.2(SULF1):c.2194C>T (p.Arg732Trp)	rs754254864	0.00003
NC_000005.10:g.(?_11732115)_(11732292_?)del
NM_001145715.3(KPNA7):c.865G>C (p.Val289Leu)	rs191355534

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