"GeneDx"[submitter] AND "LOC130061617"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1265446	NC_000017.11:g.74748373T>C	LOC130061617, NHERF1 +1 more	Single nucleotide variant	not provided	GBenign
Select item 1247073	NC_000017.11:g.74748444A>C	LOC130061617, NHERF1 +1 more	Single nucleotide variant	not provided	GBenign
Select item 1316461	NC_000017.11:g.74748473G>A	LOC130061617, NHERF1 +1 more	Single nucleotide variant	not provided	GLikely benign
Select item 1277585	NM_004252.5(NHERF1):c.-188G>C	LOC130061617, MIR3615 +2 more	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 2572959	NM_004252.5(NHERF1):c.-116C>T	LOC130061617, NHERF1 +1 more	Single nucleotide variant (5 prime UTR variant)	not provided	GLikely benign
Select item 1315840	NM_004252.5(NHERF1):c.-75G>A	LOC130061617, NHERF1 +1 more	Single nucleotide variant (5 prime UTR variant)	not provided	GLikely benign
Select item 1316123	NM_004252.5(NHERF1):c.-43C>A	LOC130061617, NHERF1 +1 more	Single nucleotide variant (5 prime UTR variant)	not provided	GLikely benign

ClinVar