List of variants in gene LRPPRC reported as benign by Illumina Laboratory Services, Illumina

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: 27

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HGVS	dbSNP	gnomAD frequency
NM_133259.4(LRPPRC):c.246G>A (p.Gln82=)	rs6741066	0.69341
NM_133259.4(LRPPRC):c.*1665C>T	rs1139250	0.63748
NM_133259.4(LRPPRC):c.1068A>G (p.Gln356=)	rs4953042	0.14931
NM_133259.4(LRPPRC):c.3900+14C>T	rs3795859	0.10271
NM_133259.4(LRPPRC):c.3900+15C>T	rs76850904	0.09620
NM_133259.4(LRPPRC):c.*556A>T	rs1136998	0.07663
NM_133259.3(LRPPRC):c.-45G>A	rs11124961	0.05742
NM_133259.4(LRPPRC):c.3570-3C>T	rs35113761	0.02876
NM_133259.4(LRPPRC):c.41C>G (p.Ala14Gly)	rs114205971	0.02459
NM_133259.4(LRPPRC):c.1888C>T (p.Leu630=)	rs35881858	0.02080
NM_133259.4(LRPPRC):c.*2176A>T	rs73924082	0.01948
NM_133259.4(LRPPRC):c.1432A>G (p.Thr478Ala)	rs35035668	0.01872
NM_133259.4(LRPPRC):c.*825A>G	rs17031753	0.01776
NM_133259.4(LRPPRC):c.*1088G>C	rs79225555	0.01767
NM_133259.4(LRPPRC):c.*1371C>T	rs111381413	0.01377
NM_133259.4(LRPPRC):c.2562A>G (p.Val854=)	rs4494798	0.01150
NM_133259.4(LRPPRC):c.3595A>G (p.Asn1199Asp)	rs113974315	0.00985
NM_133259.4(LRPPRC):c.*1343G>C	rs75002669	0.00947
NM_133259.4(LRPPRC):c.2481A>G (p.Pro827=)	rs115993634	0.00825
NM_133259.4(LRPPRC):c.*734A>G	rs114517881	0.00810
NM_133259.4(LRPPRC):c.1529C>G (p.Ala510Gly)	rs115693730	0.00414
NM_133259.4(LRPPRC):c.*1335T>C	rs76970610	0.00348
NM_133259.4(LRPPRC):c.2325A>G (p.Lys775=)	rs139634347	0.00249
NM_133259.4(LRPPRC):c.-11A>G	rs188424940	0.00066
NM_133259.4(LRPPRC):c.*2041C>T	rs7581308
NM_133259.4(LRPPRC):c.1491A>T (p.Glu497Asp)	rs571886021
NM_133259.4(LRPPRC):c.1677+11C>G	rs58811869

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