List of variants in gene ZFYVE26 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: 25

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HGVS	dbSNP	gnomAD frequency
NM_015346.4(ZFYVE26):c.*1409C>T	rs10288	0.94789
NM_015346.4(ZFYVE26):c.*1582G>A	rs8017209	0.94782
NM_015346.4(ZFYVE26):c.5672A>G (p.Asn1891Ser)	rs3742883	0.93729
NM_015346.4(ZFYVE26):c.*1361T>C	rs1044126	0.43636
NM_015346.4(ZFYVE26):c.*365A>G	rs12879105	0.41164
NM_015346.4(ZFYVE26):c.*1740C>A	rs9449	0.17216
NM_015346.4(ZFYVE26):c.2559G>A (p.Leu853=)	rs7143196	0.14152
NM_015346.4(ZFYVE26):c.2692A>T (p.Thr898Ser)	rs17192170	0.09199
NM_015346.4(ZFYVE26):c.3365C>T (p.Ala1122Val)	rs3742884	0.04741
NM_015346.4(ZFYVE26):c.3308C>T (p.Pro1103Leu)	rs3742885	0.04730
NM_015346.4(ZFYVE26):c.3118T>A (p.Ser1040Thr)	rs112787369	0.03993
NM_015346.4(ZFYVE26):c.3757C>T (p.Leu1253=)	rs34296097	0.03528
NM_015346.4(ZFYVE26):c.1224G>T (p.Gly408=)	rs17104689	0.03409
NM_015346.4(ZFYVE26):c.6921C>T (p.Ser2307=)	rs35917338	0.01911
NM_015346.4(ZFYVE26):c.*1133A>G	rs73276687	0.01855
NM_015346.4(ZFYVE26):c.7407T>C (p.Asp2469=)	rs35106153	0.01846
NM_015346.4(ZFYVE26):c.5784T>C (p.Tyr1928=)	rs34852231	0.01623
NM_015346.4(ZFYVE26):c.6987-3C>T	rs76728509	0.01610
NM_015346.4(ZFYVE26):c.*1768C>T	rs57048278	0.01228
NM_015346.4(ZFYVE26):c.5612G>A (p.Cys1871Tyr)	rs61746722	0.00962
NM_015346.4(ZFYVE26):c.6405G>A (p.Leu2135=)	rs76327447	0.00220
NM_015346.4(ZFYVE26):c.453C>T (p.Ser151=)	rs75391113	0.00203
NM_015346.4(ZFYVE26):c.1933A>G (p.Met645Val)	rs77129887	0.00201
NM_015346.4(ZFYVE26):c.3210C>G (p.Pro1070=)	rs7156492
NM_015346.4(ZFYVE26):c.4370G>A (p.Cys1457Tyr)	rs2235967

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