ClinVar Miner

List of variants in gene NEXMIF reported as benign for X-linked disease

Included ClinVar conditions (313):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 4
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HGVS dbSNP
NM_001008537.3(NEXMIF):c.2139G>A (p.Glu713=) rs139194076
NM_001008537.3(NEXMIF):c.2849A>T (p.Tyr950Phe) rs373566578
NM_001008537.3(NEXMIF):c.3361C>T (p.Arg1121Trp) rs199579887
NM_001008537.3(NEXMIF):c.3753A>G (p.Ile1251Met) rs143365662

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