List of variants in gene combination LOC100287944, POLR3B reported as 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_018082.6(POLR3B):c.3099-245A>G	rs2288268	0.27967
NM_018082.6(POLR3B):c.3396T>C (p.Asn1132=)	rs13561	0.24486
NM_018082.6(POLR3B):c.3098+38A>C	rs12300729	0.02569
NM_018082.6(POLR3B):c.2985-41A>G	rs115506843	0.01799
NM_018082.6(POLR3B):c.3272+177T>C	rs76444679	0.01786
NM_018082.6(POLR3B):c.3099-85C>T	rs115674949	0.01675
NM_018082.6(POLR3B):c.3098+147A>G	rs7962691	0.01445
NM_018082.6(POLR3B):c.2984+231dup	rs368051175

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