List of variants in gene SFXN4 reported as benign for Growth and developmental delay-hypotonia-vision impairment-lactic acidosis syndrome

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_213649.2(SFXN4):c.472-24T>A	rs2420494	0.98520
NM_213649.2(SFXN4):c.354A>G (p.Ala118=)	rs2181118	0.98355
NM_213649.2(SFXN4):c.415-6C>T	rs2275111	0.48143
NM_213649.2(SFXN4):c.258A>G (p.Gln86=)	rs10749291	0.46610
NM_213649.2(SFXN4):c.361-42C>T	rs2275112	0.29607
NM_213649.2(SFXN4):c.617-3C>T	rs17668734	0.28961

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