List of variants in gene combination SNHG14, SNRPN reported as uncertain significance for Autism spectrum disorder

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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: 7

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HGVS	dbSNP	gnomAD frequency
NM_022807.5(SNRPN):c.-584A>G	rs58890023	0.00181
NM_022807.5(SNRPN):c.-636C>A	rs886051013	0.00002
NM_022807.5(SNRPN):c.-504-12T>C	rs886051015	0.00001
NM_022807.5(SNRPN):c.-819C>A	rs886051012	0.00001
NM_022807.5(SNRPN):c.-823T>C	rs886051011	0.00001
NM_022807.5(SNRPN):c.-596del	rs886051014
NM_022807.5(SNRPN):c.-841T>A	rs886051010

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