List of variants in gene RSRC1 reported as uncertain significance for autosomal recessive non-syndromic intellectual disability

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001271838.2(RSRC1):c.196C>T (p.Arg66Cys)	rs772577036	0.00002
NM_001271838.2(RSRC1):c.11G>A (p.Arg4Gln)	rs749608883	0.00001
NM_001271838.2(RSRC1):c.230_231delinsAA (p.Gly77Glu)

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