List of variants in gene SUFU reported as benign 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
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 23

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HGVS	dbSNP	gnomAD frequency
NM_016169.4(SUFU):c.183-126G>C	rs10748822	0.99929
NM_016169.4(SUFU):c.*20T>G	rs4917980	0.99823
NM_016169.4(SUFU):c.757-75A>G	rs10786690	0.99262
NM_016169.4(SUFU):c.1365+19T>C	rs12414407	0.68304
NM_016169.4(SUFU):c.182+16C>T	rs2274351	0.46492
NM_016169.4(SUFU):c.1296+1565G>A	rs10786698	0.46247
NM_016169.4(SUFU):c.317+157G>A	rs2281880	0.46118
NM_016169.4(SUFU):c.1157+99G>A	rs2001389	0.44703
NM_016169.4(SUFU):c.*1122C>T	rs11596235	0.23520
NM_016169.4(SUFU):c.*2585T>C	rs11191355	0.20858
NM_016169.4(SUFU):c.*2668C>T	rs11594179	0.16920
NM_016169.4(SUFU):c.1299T>C (p.Ile433=)	rs17114803	0.15159
NM_016169.4(SUFU):c.*1373C>T	rs17114808	0.14776
NM_016169.4(SUFU):c.*391A>G	rs2298278	0.14670
NM_016169.4(SUFU):c.*1715A>G	rs11818043	0.14606
NM_016169.4(SUFU):c.1022+49T>C	rs3824756	0.14597
NM_016169.4(SUFU):c.*1633C>T	rs17114810	0.14323
NM_016169.4(SUFU):c.911-337C>T	rs11815464	0.04566
NM_016169.4(SUFU):c.*118C>T	rs2298277	0.00835
NM_016169.4(SUFU):c.1023-210G>C	rs7093285
NM_016169.4(SUFU):c.1158-101C>T	rs78549129
NM_016169.4(SUFU):c.183-49G>C	rs2281879
NM_016169.4(SUFU):c.183-66C>A	rs185072800

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