ClinVar Miner

List of variants reported as benign for autosomal recessive severe congenital neutropenia due to JAGN1 deficiency by Invitae

Included ClinVar conditions (1):
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ClinVar version:
Total variants: 4
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NM_032492.4(JAGN1):c.21G>C (p.Pro7=) rs138937423
NM_032492.4(JAGN1):c.244A>G (p.Ile82Val) rs35365817
NM_032492.4(JAGN1):c.403G>A (p.Ala135Thr) rs61746084
NM_032492.4(JAGN1):c.498C>T (p.Ser166=) rs61738795

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