ClinVar Miner

List of variants in gene INPPL1, LOC130006327 studied for opsismodysplasia

Included ClinVar conditions (1):

Opsismodysplasia

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001567.3(INPPL1):c.[1687_1691delACCTC;35dupG]
NM_001567.3(INPPL1):c.[24_39del16;753G>C]
NM_001567.4(INPPL1):c.24_39del (p.Gly9fs)	rs878853119

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