List of variants in gene SUFU reported as uncertain significance for Medulloblastoma; Familial meningioma; Joubert syndrome 32; Basal cell nevus syndrome 2

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.1105G>A (p.Val369Ile)	rs149449923	0.00006
NM_016169.4(SUFU):c.992G>A (p.Arg331Gln)	rs141359583	0.00005
NM_016169.4(SUFU):c.169A>G (p.Ile57Val)	rs377614167	0.00002
NM_016169.4(SUFU):c.275G>C (p.Ser92Thr)	rs746322193	0.00002
NM_016169.4(SUFU):c.928G>A (p.Glu310Lys)	rs376797758	0.00002
NM_016169.4(SUFU):c.1157G>A (p.Arg386Lys)	rs767814106	0.00001
NM_016169.4(SUFU):c.1429G>A (p.Val477Met)	rs1060501117	0.00001
NM_016169.4(SUFU):c.529A>G (p.Met177Val)	rs758672583	0.00001
NM_016169.4(SUFU):c.601G>A (p.Val201Ile)	rs147695965	0.00001
NM_016169.4(SUFU):c.1085G>C (p.Arg362Pro)

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