Related gene-specific medical variations for Gene (Select 655) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3064817	NM_001719.3(BMP7):c.866G>A (p.Arg289His)	BMP7 (R289H)	Single nucleotide variant (missense variant)	Nephrotic syndrome, type 12	GUncertain significance
Select item 2688672	NM_001719.3(BMP7):c.1156A>G (p.Ile386Val)	BMP7 (I386V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2498886	NM_001719.3(BMP7):c.-145G>A	BMP7, LOC109461473	Single nucleotide variant (5 prime UTR variant)	not provided	GLikely benign
Select item 1316341	NM_001719.3(BMP7):c.-146C>T	BMP7, LOC109461473	Single nucleotide variant (5 prime UTR variant)	not provided	GLikely benign
Select item 1276354	NM_001719.3(BMP7):c.-363C>T	BMP7, LOC109461473 +1 more	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 809278	GRCh37/hg19 20q13.31(chr20:55758778-55758975)x1	BMP7	Copy number loss	not provided	GLikely benign

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