List of variants reported as benign for Severe combined immunodeficiency due to LCK deficiency

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_005356.5(LCK):c.378-11G>T	rs11576030	0.01729
NM_005356.5(LCK):c.134G>A (p.Arg45Gln)	rs145088108	0.01058
NM_005356.5(LCK):c.888A>G (p.Gln296=)	rs35029770	0.00693
NM_005356.5(LCK):c.161C>G (p.Ser54Cys)	rs147431889	0.00379
NM_005356.5(LCK):c.528G>A (p.Glu176=)	rs139568272	0.00036
NM_005356.5(LCK):c.1328-7C>T	rs577301476
NM_005356.5(LCK):c.171G>A (p.Pro57=)	rs528967735

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