List of variants in gene combination LOC126861980, SMOC1 reported as pathogenic for Microphthalmia with limb anomalies

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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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001034852.3(SMOC1):c.709G>T (p.Glu237Ter)	rs1566709754
NM_001034852.3(SMOC1):c.718C>T (p.Gln240Ter)	rs376672665
NM_001034852.3(SMOC1):c.857G>A (p.Arg286His)	rs1365818420

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