List of variants in gene SUFU reported as benign for not provided

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: 30

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HGVS	dbSNP	gnomAD frequency
NM_016169.4(SUFU):c.757-75A>G	rs10786690	0.99223
NM_016169.4(SUFU):c.1365+19T>C	rs12414407	0.68248
NM_016169.4(SUFU):c.182+16C>T	rs2274351	0.46492
NM_016169.4(SUFU):c.317+157G>A	rs2281880	0.46118
NM_016169.4(SUFU):c.1296+1565G>A	rs10786698	0.45617
NM_016169.4(SUFU):c.1157+99G>A	rs2001389	0.44703
NM_016169.4(SUFU):c.455-215_455-214insCATTT	rs3839934	0.44353
NM_016169.4(SUFU):c.317+241G>A	rs10883728	0.35528
NM_016169.4(SUFU):c.182+189C>T	rs3808934	0.35481
NM_016169.4(SUFU):c.183-300T>C	rs12767131	0.22903
NM_016169.4(SUFU):c.1299T>C (p.Ile433=)	rs17114803	0.14628
NM_016169.4(SUFU):c.1022+49T>C	rs3824756	0.14597
NM_016169.4(SUFU):c.183-67del	rs139516830	0.10605
NM_016169.4(SUFU):c.911-337C>T	rs11815464	0.04566
NM_016169.4(SUFU):c.1018G>T (p.Ala340Ser)	rs34135067	0.00646
NM_016169.4(SUFU):c.210T>C (p.Tyr70=)	rs35166585	0.00430
NM_016169.4(SUFU):c.*20=	rs4917980	0.00177
NM_016169.4(SUFU):c.910+14C>T	rs202247757	0.00139
NM_016169.4(SUFU):c.600C>T (p.Ile200=)	rs149513330	0.00116
NM_016169.4(SUFU):c.1084C>T (p.Arg362Cys)	rs36049457	0.00039
NM_016169.4(SUFU):c.255C>T (p.Pro85=)	rs113671745	0.00016
NM_016169.4(SUFU):c.1272C>T (p.Tyr424=)	rs771084342	0.00009
NM_016169.4(SUFU):c.183-4G>A	rs766044613	0.00005
NM_016169.4(SUFU):c.474G>A (p.Gly158=)	rs375178556	0.00003
NM_016169.4(SUFU):c.1023-210G>C	rs7093285
NM_016169.4(SUFU):c.1158-101C>T	rs78549129
NM_016169.4(SUFU):c.1296+1378G>T	rs10786697
NM_016169.4(SUFU):c.183-126G>C	rs10748822
NM_016169.4(SUFU):c.183-49G>C	rs2281879
NM_016169.4(SUFU):c.183-66C>A	rs185072800

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