ClinVar Miner

List of variants in gene combination ASTN2, TRIM32 reported as likely pathogenic by SN ONGC Dept of Genetics and Molecular biology Vision Research Foundation

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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_012210.4(TRIM32):c.370C>T (p.Arg124Trp)	rs572052810	0.00002
NM_012210.4(TRIM32):c.722A>G (p.Tyr241Cys)	rs1860996799

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