Related gene-specific medical variations for Gene (Select 55237) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1326415	NC_000014.9:g.74303036A>G	ABCD4, LOC130056092 +1 more	Single nucleotide variant (genic upstream transcript variant)	not provided	GLikely benign
Select item 1300997	NC_000014.9:g.74303196T>A	ABCD4, LOC130056092 +1 more	Single nucleotide variant	not provided	GLikely benign
Select item 1300480	NC_000014.9:g.74303033G>C	ABCD4, LOC130056092 +1 more	Single nucleotide variant (genic upstream transcript variant)	not provided	GLikely benign
Select item 1234864	NC_000014.9:g.74303274G>A	ABCD4, LOC130056092 +1 more	Single nucleotide variant	not provided	GBenign
Select item 1212397	NC_000014.9:g.74303027G>A	LOC130056092, ABCD4 +1 more	Single nucleotide variant (genic upstream transcript variant)	not provided	GLikely benign
Select item 1181620	NC_000014.9:g.74303138C>T	LOC130056092, ABCD4 +1 more	Single nucleotide variant	not provided	GBenign

ClinVar