List of variants in gene SUFU reported as likely benign 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: 26

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HGVS	dbSNP	gnomAD frequency
NM_016169.4(SUFU):c.1365+103G>T	rs41297161	0.02069
NM_016169.4(SUFU):c.1296+1793C>T	rs149768712	0.01010
NM_016169.4(SUFU):c.1023-23C>G	rs117407459	0.01001
NM_016169.4(SUFU):c.1157+246T>G	rs2298281	0.00982
NM_016169.4(SUFU):c.*205G>A	rs115428806	0.00961
NM_016169.4(SUFU):c.756+245T>C	rs78247976	0.00958
NM_016169.4(SUFU):c.598-68G>C	rs77555631	0.00950
NM_016169.4(SUFU):c.1296+1423G>A	rs116676843	0.00949
NM_016169.4(SUFU):c.1296+1824C>T	rs78378878	0.00948
NM_016169.4(SUFU):c.455-143C>T	rs73338680	0.00944
NM_016169.4(SUFU):c.318-245T>C	rs117516904	0.00825
NM_016169.4(SUFU):c.1291T>C (p.Leu431=)	rs141950577	0.00487
NM_016169.4(SUFU):c.1296+177C>T	rs186697227	0.00484
NM_016169.4(SUFU):c.757-120G>A	rs142512844	0.00482
NM_016169.4(SUFU):c.210T>C (p.Tyr70=)	rs35166585	0.00430
NM_016169.4(SUFU):c.1157+75C>T	rs137942998	0.00341
NM_016169.4(SUFU):c.318-53G>T	rs115076998	0.00314
NM_016169.4(SUFU):c.528C>T (p.His176=)	rs150569584	0.00148
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.318-17C>A	rs201198734	0.00029
NM_016169.4(SUFU):c.537G>A (p.Leu179=)	rs139580429	0.00004
NM_016169.4(SUFU):c.1157+6C>T	rs535323089	0.00001
NM_016169.4(SUFU):c.683+17G>A	rs1027742260	0.00001
NM_016169.4(SUFU):c.*6G>A	rs375366321
NM_016169.4(SUFU):c.1296+1355C>T	rs75879889

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