List of variants in gene combination ASIC4, SPEG reported as benign for autosomal recessive disease

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_005876.5(SPEG):c.9462-27C>T	rs907146	0.96294
NM_005876.5(SPEG):c.9236A>G (p.His3079Arg)	rs12464085	0.38593
NM_005876.5(SPEG):c.8368A>G (p.Arg2790Gly)	rs55760516	0.37734
NM_005876.5(SPEG):c.7839G>A (p.Pro2613=)	rs875098	0.25609
NM_005876.5(SPEG):c.9390G>T (p.Pro3130=)	rs12473286	0.25371
NM_005876.5(SPEG):c.6566C>T (p.Pro2189Leu)	rs10755037	0.25298
NM_005876.5(SPEG):c.8059C>A (p.Pro2687Thr)	rs13026308	0.10397

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