List of variants in gene combination LOC130004614, SUFU reported as uncertain significance by GeneDx

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_016169.4(SUFU):c.50C>T (p.Ala17Val)	rs12780580	0.00023
NM_016169.4(SUFU):c.38C>T (p.Thr13Ile)	rs768935165	0.00006
NM_016169.4(SUFU):c.43C>A (p.Pro15Thr)	rs761921681	0.00005
NM_016169.4(SUFU):c.67C>T (p.Pro23Ser)	rs766666529	0.00002
NM_016169.4(SUFU):c.32G>A (p.Gly11Asp)	rs1227379293	0.00001
NM_016169.4(SUFU):c.45C>T (p.Pro15=)	rs767543227	0.00001
NM_016169.4(SUFU):c.46C>A (p.Pro16Thr)	rs978312925	0.00001
NM_016169.4(SUFU):c.103C>T (p.His35Tyr)	rs2135598180
NM_016169.4(SUFU):c.44C>T (p.Pro15Leu)	rs28942088
NM_016169.4(SUFU):c.50C>A (p.Ala17Asp)

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