ClinVar Miner

List of variants in gene combination SNHG14, SNRPN, SNURF reported as likely benign for Autism spectrum disorder

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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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_003097.6(SNRPN):c.-89T>C	rs705	0.53733
NM_003097.6(SNRPN):c.-39G>A	rs75184959	0.01903

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