List of variants in gene DNAI2 reported as likely benign for not specified

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: 18

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HGVS	dbSNP	gnomAD frequency
NM_023036.6(DNAI2):c.725-27C>T	rs72848284	0.02780
NM_023036.6(DNAI2):c.1408G>A (p.Gly470Ser)	rs115299472	0.00205
NM_023036.6(DNAI2):c.1715C>T (p.Pro572Leu)	rs151241589	0.00081
NM_023036.6(DNAI2):c.1380G>T (p.Val460=)	rs148947094	0.00043
NM_023036.6(DNAI2):c.1574C>T (p.Ala525Val)	rs145602856	0.00036
NM_023036.6(DNAI2):c.571C>T (p.Pro191Ser)	rs201457010	0.00021
NM_023036.6(DNAI2):c.*18C>T	rs369270232	0.00011
NM_023036.6(DNAI2):c.*22G>A	rs139420980	0.00004
NM_023036.6(DNAI2):c.1011C>T (p.Thr337=)	rs768490008	0.00004
NM_023036.6(DNAI2):c.1446G>T (p.Ser482=)	rs368217836	0.00004
NM_023036.6(DNAI2):c.891G>A (p.Met297Ile)	rs750750518	0.00004
NM_023036.6(DNAI2):c.933G>A (p.Lys311=)	rs570168701	0.00004
NM_023036.6(DNAI2):c.43G>A (p.Gly15Arg)	rs758997612	0.00001
NM_023036.6(DNAI2):c.45G>A (p.Gly15=)	rs751121542	0.00001
NM_023036.6(DNAI2):c.467+10T>C	rs377310209	0.00001
NM_023036.6(DNAI2):c.1348-39CT[2]	rs35732837
NM_023036.6(DNAI2):c.258C>T (p.Asn86=)	rs886038678
NM_023036.6(DNAI2):c.981T>C (p.Ser327=)	rs886038679

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