List of variants in gene ITGA7 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: 23

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HGVS	dbSNP	gnomAD frequency
NM_002206.3(ITGA7):c.1282-11T>C	rs2293412	0.58963
NM_002206.3(ITGA7):c.334+19A>G	rs2293413	0.49590
NM_002206.3(ITGA7):c.1952G>A (p.Arg651His)	rs1800974	0.48530
NM_002206.3(ITGA7):c.3184-12G>C	rs3852533	0.47439
NM_002206.3(ITGA7):c.415-10C>T	rs11171661	0.06475
NM_002206.3(ITGA7):c.810G>A (p.Gly270=)	rs3847675	0.05834
NM_002206.3(ITGA7):c.3018C>G (p.Ser1006=)	rs17117883	0.05018
NM_002206.3(ITGA7):c.824G>A (p.Arg275His)	rs74867235	0.03438
NM_002206.3(ITGA7):c.1617G>T (p.Gln539His)	rs61733963	0.01753
NM_002206.3(ITGA7):c.3144G>C (p.Gly1048=)	rs62648071	0.01749
NM_002206.3(ITGA7):c.1567+12C>T	rs79849707	0.01666
NM_002206.3(ITGA7):c.1965T>C (p.Cys655=)	rs7971022	0.01436
NM_002206.3(ITGA7):c.46T>G (p.Cys16Gly)	rs142060614	0.00719
NM_002206.3(ITGA7):c.1281+13G>A	rs143895796	0.00701
NM_002206.3(ITGA7):c.459C>G (p.Ile153Met)	rs149000088	0.00672
NM_002206.3(ITGA7):c.1609C>T (p.Arg537Trp)	rs61733050	0.00636
NM_002206.3(ITGA7):c.3384C>T (p.Pro1128=)	rs148170949	0.00509
NM_002206.3(ITGA7):c.2701A>G (p.Ile901Val)	rs113651939	0.00295
NM_002206.3(ITGA7):c.3058-6C>T	rs201070308	0.00252
NM_002206.3(ITGA7):c.791-7C>T	rs144699549	0.00087
NM_002206.3(ITGA7):c.999-4A>G	rs370741662	0.00033
NM_002206.3(ITGA7):c.285G>T (p.Pro95=)	rs17854601
NM_002206.3(ITGA7):c.671-5C>A	rs180841797

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