List of variants reported as uncertain significance for Familial cold autoinflammatory syndrome 2 by Fulgent Genetics, Fulgent Genetics

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_144687.4(NLRP12):c.850C>T (p.Arg284Ter)	rs104895564	0.00044
NM_144687.4(NLRP12):c.536C>T (p.Thr179Ile)	rs145156267	0.00011
NM_144687.4(NLRP12):c.1886C>A (p.Ala629Asp)	rs146250162	0.00007
NM_144687.4(NLRP12):c.2072+2_2072+3insTT	rs104895565
NM_144687.4(NLRP12):c.2110C>T (p.His704Tyr)	rs1380366925
NM_144687.4(NLRP12):c.3088C>T (p.Arg1030Ter)	rs201619538

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