List of variants in gene SLX4 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: 16

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HGVS	dbSNP	gnomAD frequency
NM_032444.4(SLX4):c.1371T>G (p.Asn457Lys)	rs74319927	0.06397
NM_032444.4(SLX4):c.1153C>A (p.Pro385Thr)	rs115694169	0.00968
NM_032444.4(SLX4):c.5501A>G (p.Asn1834Ser)	rs111738042	0.00575
NM_032444.4(SLX4):c.*1041A>G	rs117958592	0.00304
NM_032444.4(SLX4):c.3857C>T (p.Ala1286Val)	rs149011965	0.00302
NM_032444.4(SLX4):c.*658T>C	rs541410329	0.00227
NM_032444.4(SLX4):c.4648C>T (p.Arg1550Trp)	rs77021998	0.00214
NM_032444.4(SLX4):c.-381A>G	rs375326827	0.00205
NM_032444.4(SLX4):c.422G>T (p.Gly141Val)	rs77306735	0.00131
NM_032444.4(SLX4):c.2844G>A (p.Ala948=)	rs376877866	0.00053
NM_032444.4(SLX4):c.*1035A>G	rs149634682	0.00034
NM_032444.4(SLX4):c.2628C>T (p.Asp876=)	rs201279467	0.00016
NM_032444.4(SLX4):c.1925-13A>T	rs201324113	0.00011
NM_032444.4(SLX4):c.3762G>A (p.Ser1254=)	rs3810814	0.00007
NM_032444.4(SLX4):c.3245A>G (p.Gln1082Arg)	rs368657696	0.00001
NM_032444.4(SLX4):c.*128A>G	rs528843807

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