ClinVar Miner

List of variants reported as likely benign for opsismodysplasia

Included ClinVar conditions (1):

Opsismodysplasia

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Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001567.4(INPPL1):c.909G>C (p.Lys303Asn)	rs17847215	0.00985
NM_001567.4(INPPL1):c.36C>A (p.Gly12=)	rs1011212998	0.00033
NM_001567.4(INPPL1):c.465G>A (p.Gly155=)	rs760197203	0.00001

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