List of variants in gene HNRNPU 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: 14

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HGVS	dbSNP	gnomAD frequency
NM_031844.3(HNRNPU):c.261G>A (p.Glu87=)	rs6675421	0.28406
NM_031844.3(HNRNPU):c.877+71T>A	rs12124462	0.27768
NM_031844.3(HNRNPU):c.1495-113G>C	rs9730334	0.21984
NM_031844.3(HNRNPU):c.1615-127A>G	rs1874393	0.15218
NM_031844.3(HNRNPU):c.877+70G>A	rs58736171	0.13080
NM_031844.3(HNRNPU):c.1117+24T>G	rs73128486	0.06036
NM_031844.3(HNRNPU):c.1615-209C>T	rs76169958	0.05593
NM_031844.3(HNRNPU):c.1117+153G>A	rs79834162	0.02311
NM_031844.3(HNRNPU):c.2352+14A>T	rs57080269	0.02104
NM_031844.3(HNRNPU):c.803+11C>T	rs74152197	0.01701
NC_000001.11:g.244864715T>G	rs116239278	0.01649
NM_031844.3(HNRNPU):c.1743+10A>C	rs75053711	0.00248
NM_031844.3(HNRNPU):c.1118-30C>A	rs145042684
NM_031844.3(HNRNPU):c.2167+39C>A	rs190132789

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