List of variants in gene combination LOC129935618, WNT10A reported as uncertain significance for SchC6pf-Schulz-Passarge syndrome

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_025216.2(WNT10A):c.-341A>G	rs762914440	0.00028
NM_025216.2(WNT10A):c.-249G>C	rs571829301	0.00023
NM_025216.2(WNT10A):c.-270G>C	rs774035749	0.00010
NM_025216.2(WNT10A):c.-285C>T	rs886055636	0.00002
NM_025216.2(WNT10A):c.-370C>A	rs886055634	0.00002
NM_025216.2(WNT10A):c.-358G>A	rs886055635	0.00001
NM_025216.2(WNT10A):c.-433C>G	rs886055633

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