"Illumina Laboratory Services, Illumina"[submitter] AND "LOC129935618" - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 334378	NM_025216.2(WNT10A):c.-433C>G	LOC129935618, WNT10A	Single nucleotide variant (genic upstream transcript variant)	SchC6pf-Schulz-Passarge syndrome +2 more	GUncertain significance
Select item 334379	NM_025216.2(WNT10A):c.-400T>G	LOC129935618, WNT10A	Single nucleotide variant (genic upstream transcript variant)	Odonto-onycho-dermal dysplasia +2 more	GLikely benign
Select item 334380	NM_025216.2(WNT10A):c.-370C>A	LOC129935618, WNT10A	Single nucleotide variant (genic upstream transcript variant)	Odonto-onycho-dermal dysplasia +2 more	GUncertain significance
Select item 334381	NM_025216.2(WNT10A):c.-358G>A	LOC129935618, WNT10A	Single nucleotide variant (genic upstream transcript variant)	SchC6pf-Schulz-Passarge syndrome +2 more	GUncertain significance
Select item 334382	NM_025216.2(WNT10A):c.-341A>G	LOC129935618, WNT10A	Single nucleotide variant (genic upstream transcript variant)	SchC6pf-Schulz-Passarge syndrome +2 more	GUncertain significance
Select item 334383	NM_025216.2(WNT10A):c.-312C>T	LOC129935618, WNT10A	Single nucleotide variant (genic upstream transcript variant)	SchC6pf-Schulz-Passarge syndrome +2 more	GLikely benign
Select item 334384	NM_025216.2(WNT10A):c.-285C>T	LOC129935618, WNT10A	Single nucleotide variant (genic upstream transcript variant)	SchC6pf-Schulz-Passarge syndrome +2 more	GUncertain significance
Select item 334385	NM_025216.2(WNT10A):c.-270G>C	LOC129935618, WNT10A	Single nucleotide variant (genic upstream transcript variant)	Odonto-onycho-dermal dysplasia +2 more	GUncertain significance
Select item 334386	NM_025216.2(WNT10A):c.-249G>C	LOC129935618, WNT10A	Single nucleotide variant (genic upstream transcript variant)	Odonto-onycho-dermal dysplasia +3 more	GUncertain significance