Related gene-specific medical variations for Gene (Select 143162) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3097000	NM_001018071.4(FRMPD2):c.2264C>G (p.Ala755Gly)	FRMPD2, LOC126860930 (A755G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 395331	GRCh37/hg19 10q11.22(chr10:49367155-49382926)x3	FRMPD2	Copy number gain	See cases	GBenign/Likely benign
Select item 394834	GRCh37/hg19 10q11.22(chr10:49367155-49392896)x3	FRMPD2	Copy number gain	See cases	GBenign
Select item 394824	GRCh37/hg19 10q11.22(chr10:49367155-49440299)x3	FRMPD2	Copy number gain	See cases	GLikely benign

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