List of variants in gene INPPL1 reported as likely pathogenic for opsismodysplasia

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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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001567.4(INPPL1):c.1945C>T (p.Arg649Ter)
NM_001567.4(INPPL1):c.2213-2A>C	rs1948918434
NM_001567.4(INPPL1):c.2356C>T (p.Gln786Ter)	rs2135438529
NM_001567.4(INPPL1):c.3466del (p.Arg1156fs)	rs760925109
NM_001567.4(INPPL1):c.3549_3550insA (p.Glu1184fs)	rs1949036008

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