List of variants in gene SZT2 reported as benign by PreventionGenetics, part of Exact Sciences

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: 22

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HGVS	dbSNP	gnomAD frequency
NM_001365999.1(SZT2):c.3194G>A (p.Arg1065Gln)	rs2782646	0.33898
NM_001365999.1(SZT2):c.8626-3T>C	rs2255632	0.32528
NM_001365999.1(SZT2):c.6034+11A>C	rs2039531	0.31639
NM_001365999.1(SZT2):c.1336C>T (p.Pro446Ser)	rs2782643	0.31563
NM_001365999.1(SZT2):c.7356A>G (p.Glu2452=)	rs2027130	0.31124
NM_001365999.1(SZT2):c.5385T>G (p.Ser1795=)	rs12129487	0.03117
NM_001365999.1(SZT2):c.6888C>T (p.Cys2296=)	rs72671125	0.01988
NM_001365999.1(SZT2):c.9441-12C>T	rs115595942	0.01911
NM_001365999.1(SZT2):c.5535T>G (p.Ser1845Arg)	rs114759137	0.01542
NM_001365999.1(SZT2):c.2929+9G>A	rs114863461	0.01479
NM_001365999.1(SZT2):c.5198G>A (p.Arg1733His)	rs147797700	0.01015
NM_001365999.1(SZT2):c.2578G>A (p.Glu860Lys)	rs143992266	0.00936
NM_001365999.1(SZT2):c.7211-13C>G	rs116454519	0.00705
NM_001365999.1(SZT2):c.7562T>C (p.Val2521Ala)	rs150113647	0.00337
NM_001365999.1(SZT2):c.8499+8A>C	rs182225944	0.00297
NM_001365999.1(SZT2):c.7395T>C (p.Ile2465=)	rs78858677	0.00134
NM_001365999.1(SZT2):c.3267C>T (p.Val1089=)	rs147008168	0.00125
NM_001365999.1(SZT2):c.7975-10C>T	rs181831231	0.00100
NM_001365999.1(SZT2):c.7512-3C>T	rs117106532	0.00086
NM_001365999.1(SZT2):c.8020T>C (p.Leu2674=)	rs187106999	0.00086
NM_001365999.1(SZT2):c.2550+5G>T	rs41270349
NM_001365999.1(SZT2):c.6508+16G>T	rs2782648

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