List of intergenic variants reported as benign for not provided

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: 32

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HGVS	dbSNP	gnomAD frequency
NC_000003.12:g.49095877A>G	rs9840050	0.65034
NC_000023.11:g.136644791A>G	rs3092952	0.28633
NC_000023.11:g.101832078G>C	rs6616305	0.15922
NR_163193.1(TCP10):n.623G>A	rs2345794	0.07876
NC_000004.12:g.122922970G>T	rs58090513	0.04669
NR_164162.1(GLRA4):n.697T>G	rs61732248	0.02727
NR_164162.1(GLRA4):n.750G>A	rs61749967	0.02616
NM_001047980.2(NBPF7):c.400C>T (p.Arg134Trp)	rs78204967	0.02472
NM_001047980.2(NBPF7):c.1089C>T (p.Ser363=)	rs6684816	0.02393
NC_000012.12:g.6125718G>A	rs151088025	0.02305
NM_199249.2(C19orf48):c.19G>A (p.Val7Ile)	rs7251816	0.01898
NR_164162.1(GLRA4):n.1450T>C	rs149690029	0.01800
NR_164162.1(GLRA4):n.965C>T	rs142642074	0.01734
NR_163193.1(TCP10):n.566G>A	rs201005141	0.01428
NR_164162.1(GLRA4):n.1475A>G	rs61744012	0.01070
NR_164162.1(GLRA4):n.1091C>T	rs41300882	0.00964
NR_164162.1(GLRA4):n.452C>T	rs61730416	0.00940
NM_199249.2(C19orf48):c.291C>T (p.Thr97=)	rs73586837	0.00914
NM_199249.2(C19orf48):c.308C>T (p.Pro103Leu)	rs138504348	0.00600
NR_164162.1(GLRA4):n.1383A>G	rs145491863	0.00576
NC_000016.10:g.177647G>A	rs114920844	0.00455
NR_164162.1(GLRA4):n.1525G>T	rs185557554	0.00322
NM_199249.2(C19orf48):c.279A>G (p.Ser93=)	rs149603271	0.00230
NR_164162.1(GLRA4):n.1027C>T	rs185429747	0.00120
NR_164162.1(GLRA4):n.1175G>A	rs201999101	0.00025
GRCh37/hg19 18q22.1(chr18:65255832-65686626)x3
NC_000006.12:g.79947809C>A
NC_000012.12:g.6125082T>G
NC_000012.12:g.6125524A>C
NC_000012.12:g.6125683C>T
NC_000014.9:g.100779738G>A
Single allele

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