List of variants in gene SUFU reported as uncertain significance for Gorlin 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_016169.4(SUFU):c.1058C>T (p.Thr353Met)	rs137880855	0.00015
NM_016169.4(SUFU):c.1296+1638C>T	rs368920108	0.00014
NM_016169.4(SUFU):c.183-4G>A	rs766044613	0.00005
NM_016169.4(SUFU):c.275G>C (p.Ser92Thr)	rs746322193	0.00002
NM_016169.4(SUFU):c.1177C>T (p.Arg393Trp)	rs201326378	0.00001
NM_016169.4(SUFU):c.1379A>G (p.Lys460Arg)	rs778125780	0.00001
NM_016169.4(SUFU):c.1023-3C>T	rs550262133

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