List of variants in gene LDLR reported as likely 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: 28

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HGVS	dbSNP	gnomAD frequency
NM_000527.5(LDLR):c.*1216dup	rs34113544	0.56429
NM_000527.5(LDLR):c.*2054G>A	rs28398082	0.03101
NM_000527.5(LDLR):c.*1417A>C	rs72658878	0.01310
NM_000527.5(LDLR):c.*803C>T	rs17242677	0.01212
NM_000527.5(LDLR):c.90C>T (p.Asn30=)	rs72658855	0.00965
NM_000527.5(LDLR):c.*1550A>T	rs143587805	0.00878
NM_000527.5(LDLR):c.*2111G>A	rs148054434	0.00508
NM_000527.5(LDLR):c.*1960C>T	rs8108932	0.00395
NM_000527.5(LDLR):c.*1292C>T	rs556381931	0.00379
NM_000527.5(LDLR):c.*338G>A	rs17249029	0.00235
NM_000527.5(LDLR):c.*517C>A	rs115882455	0.00227
NM_000527.5(LDLR):c.*1173G>C	rs17249379	0.00217
NM_000527.5(LDLR):c.1545C>T (p.Asn515=)	rs147896205	0.00183
NM_000527.5(LDLR):c.*1377G>A	rs563300769	0.00078
NM_000527.5(LDLR):c.*1140G>A	rs367606490	0.00019
NM_000527.5(LDLR):c.*1269G>A	rs573433655	0.00005
NM_000527.5(LDLR):c.993C>T (p.Asp331=)	rs147905921	0.00002
NM_000527.5(LDLR):c.*1232CTA[1]	rs398059563
NM_000527.5(LDLR):c.*2126G>A	rs142697277
NM_000527.5(LDLR):c.*2196TA[7]	rs3980933
NM_000527.5(LDLR):c.*223G>A	rs17243011
NM_000527.5(LDLR):c.*965C>T	rs72658874
NM_000527.5(LDLR):c.1024G>A (p.Asp342Asn)
NM_000527.5(LDLR):c.148G>T (p.Ala50Ser)	rs137853960
NM_000527.5(LDLR):c.2231G>A (p.Arg744Gln)
NM_000527.5(LDLR):c.829G>A (p.Glu277Lys)
NM_000527.5(LDLR):c.940+9C>T
NM_000527.5(LDLR):c.970G>A (p.Gly324Ser)

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