"PreventionGenetics, part of Exact Sciences"[submitter] AND "LOC106029 - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3060492	NM_016379.4(VCX3A):c.*9C>G	LOC106029240, VCX3A	Single nucleotide variant (3 prime UTR variant)	VCX3A-related disorder	GLikely benign
Select item 3058916	NM_016379.4(VCX3A):c.*8G>A	LOC106029240, VCX3A	Single nucleotide variant (3 prime UTR variant)	VCX3A-related disorder	GLikely benign
Select item 3057107	NM_016379.4(VCX3A):c.*2C>T	LOC106029240, VCX3A	Single nucleotide variant (3 prime UTR variant)	VCX3A-related disorder	GLikely benign
Select item 3047456	NM_001001888.4(VCX3B):c.288C>T (p.Ser96=)	LOC106029240, VCX3A	Single nucleotide variant (synonymous variant)	VCX3A-related disorder	GLikely benign
Select item 3030020	NM_001001888.4(VCX3B):c.249G>A (p.Glu83=)	LOC106029240, VCX3A	Single nucleotide variant (synonymous variant)	VCX3A-related disorder	GLikely benign
Select item 3034320	NM_001001888.4(VCX3B):c.222C>A (p.Pro74=)	LOC106029240, VCX3A	Single nucleotide variant (synonymous variant)	VCX3A-related disorder	GLikely benign
Select item 3042675	NM_001001888.4(VCX3B):c.93G>A (p.Pro31=)	LOC106029240, VCX3A	Single nucleotide variant (synonymous variant)	VCX3A-related disorder	GLikely benign
Select item 3056669	NM_001001888.4(VCX3B):c.15G>C (p.Pro5=)	LOC106029240, VCX3A	Single nucleotide variant (synonymous variant)	VCX3A-related disorder	GLikely benign

ClinVar