List of variants in gene combination ARID1A, LOC126805670 reported as uncertain significance for multiple congenital anomalies/dysmorphic syndrome-intellectual disability

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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: 4

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HGVS	dbSNP	gnomAD frequency
NM_006015.6(ARID1A):c.3408G>A (p.Ala1136=)	rs146598030	0.00029
NM_006015.6(ARID1A):c.3539+5G>A	rs750030197	0.00001
NM_006015.6(ARID1A):c.3487C>T (p.Pro1163Ser)
NM_006015.6(ARID1A):c.3516G>C (p.Gln1172His)

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