ClinVar Miner

List of variants in gene INPPL1, LOC130006328 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: 2

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HGVS	dbSNP	gnomAD frequency
NM_001567.4(INPPL1):c.115_128del (p.Gly39fs)	rs2135414009
NM_001567.4(INPPL1):c.94_121del (p.Glu32fs)	rs797044470

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