List of variants in gene LTBP2 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: 11

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HGVS	dbSNP	gnomAD frequency
NM_000428.3(LTBP2):c.2406T>C (p.Thr802=)	rs699374	0.35704
NM_000428.3(LTBP2):c.1287G>A (p.Leu429=)	rs61738025	0.06415
NM_000428.3(LTBP2):c.956C>A (p.Pro319Gln)	rs2304707	0.06364
NM_000428.3(LTBP2):c.2788+13C>T	rs78258030	0.03459
NM_000428.3(LTBP2):c.4782G>A (p.Val1594=)	rs2079631	0.02179
NM_000428.3(LTBP2):c.915G>A (p.Thr305=)	rs60337900	0.01390
NM_000428.3(LTBP2):c.378C>T (p.Pro126=)	rs140842900	0.00528
NM_000428.3(LTBP2):c.1399+10G>T	rs143528294	0.00488
NM_000428.3(LTBP2):c.4203G>A (p.Thr1401=)	rs150977380	0.00305
NM_000428.3(LTBP2):c.3807G>A (p.Pro1269=)	rs149953380	0.00193
NM_000428.3(LTBP2):c.2160C>T (p.Phe720=)	rs74758312	0.00023

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