List of variants in gene FRMPD4 reported as likely benign by Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center

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)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001368397.1(FRMPD4):c.388G>A (p.Ala130Thr)	rs139449383	0.00099
NM_001368397.1(FRMPD4):c.3438A>C (p.Gln1146His)	rs139151624	0.00042
NM_001368397.1(FRMPD4):c.2048A>G (p.Glu683Gly)	rs760597864	0.00004
NM_001368397.1(FRMPD4):c.3491A>T (p.Asp1164Val)	rs2147176569

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