ClinVar Miner

List of variants reported as benign for Severe combined immunodeficiency due to CARMIL2 deficiency

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001013838.3(CARMIL2):c.1440-8T>C	rs9972635	0.15291
NM_001013838.3(CARMIL2):c.688-32C>T	rs59376497	0.11931
NM_001013838.3(CARMIL2):c.4195+39C>T	rs117444844	0.02956

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