ClinVar Miner

List of variants in gene ITGA7 reported as uncertain significance by Eurofins NTD LLC (GA)

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Gene type:
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Total variants: 19
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HGVS dbSNP gnomAD frequency
NM_002206.3(ITGA7):c.2569G>A (p.Gly857Ser) rs149081471 0.00270
NM_002206.3(ITGA7):c.1606C>T (p.Leu536Phe) rs149028067 0.00083
NM_002206.3(ITGA7):c.1722C>A (p.Ala574=) rs142311782 0.00066
NM_002206.3(ITGA7):c.537G>A (p.Gly179=) rs145463677 0.00061
NM_002206.3(ITGA7):c.284C>T (p.Pro95Leu) rs143749139 0.00044
NM_002206.3(ITGA7):c.1765A>C (p.Ile589Leu) rs200065922 0.00032
NM_002206.3(ITGA7):c.1317C>T (p.Phe439=) rs200714716 0.00019
NM_002206.3(ITGA7):c.3287C>T (p.Thr1096Met) rs200485048 0.00019
NM_002206.3(ITGA7):c.892C>T (p.Arg298Cys) rs201594532 0.00019
NM_002206.3(ITGA7):c.1589C>T (p.Ala530Val) rs200267194 0.00011
NM_002206.3(ITGA7):c.1568-9A>G rs761067098 0.00005
NM_002206.3(ITGA7):c.287T>G (p.Leu96Trp) rs886042999 0.00004
NM_002206.3(ITGA7):c.518G>A (p.Arg173Gln) rs144639829 0.00002
NM_002206.3(ITGA7):c.128G>T (p.Arg43Leu) rs794726901 0.00001
NM_002206.3(ITGA7):c.1771G>A (p.Val591Met) rs774213412 0.00001
NM_002206.3(ITGA7):c.1854C>T (p.Leu618=) rs372612921
NM_002206.3(ITGA7):c.2642T>A (p.Val881Asp) rs794727321
NM_002206.3(ITGA7):c.656C>T (p.Thr219Ile) rs765610371
NM_002206.3(ITGA7):c.708C>A (p.Pro236=) rs555521550

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