List of variants in gene combination LOC130004614, SUFU reported by Breakthrough Genomics, Breakthrough Genomics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_016169.3(SUFU):c.-235T>C	rs3818470	0.35181
NM_016169.4(SUFU):c.-178C>T	rs113962600	0.05045
NC_000010.11:g.102503867T>G	rs73336657	0.04683
NM_016169.4(SUFU):c.-33C>T	rs201649559	0.00551
NM_016169.4(SUFU):c.12G>A (p.Leu4=)	rs189234140	0.00425
NM_016169.4(SUFU):c.31G>C (p.Gly11Arg)	rs1322807658
NM_016169.4(SUFU):c.37_42del (p.Thr13_Ala14del)	rs1589969829

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