List of variants in gene LDLRAP1 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: 12

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HGVS	dbSNP	gnomAD frequency
NM_015627.3(LDLRAP1):c.985_986insTG	rs10635955	0.99254
NM_015627.3(LDLRAP1):c.654A>G (p.Thr218=)	rs28969504	0.62316
NM_015627.3(LDLRAP1):c.*1755C>T	rs7491	0.53347
NM_015627.3(LDLRAP1):c.*1370G>T	rs11563	0.53028
NM_015627.3(LDLRAP1):c.604T>C (p.Ser202Pro)	rs6687605	0.47789
NM_015627.3(LDLRAP1):c.*1794G>A	rs4537542	0.03639
NM_015627.3(LDLRAP1):c.*1793C>T	rs10062	0.01400
NM_015627.3(LDLRAP1):c.*63G>A	rs62619761	0.00494
NM_015627.3(LDLRAP1):c.*596C>T	rs117614534	0.00275
NM_015627.3(LDLRAP1):c.605C>A (p.Ser202Tyr)	rs121908326	0.00147
NM_015627.3(LDLRAP1):c.*1880C>T	rs563575568	0.00007
NM_015627.3(LDLRAP1):c.*449del	rs397860393

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