ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 41
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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.824G>A (p.Arg275His) rs74867235 0.03438
NM_002206.3(ITGA7):c.1965T>C (p.Cys655=) rs7971022 0.01436
NM_002206.3(ITGA7):c.3384C>T (p.Pro1128=) rs148170949 0.00509
NM_002206.3(ITGA7):c.2644G>A (p.Glu882Lys) rs144983062 0.00347
NM_002206.3(ITGA7):c.2701A>G (p.Ile901Val) rs113651939 0.00295
NM_002206.3(ITGA7):c.2569G>A (p.Gly857Ser) rs149081471 0.00270
NM_002206.3(ITGA7):c.3058-6C>T rs201070308 0.00252
NM_002206.3(ITGA7):c.882G>A (p.Val294=) rs148190047 0.00223
NM_002206.3(ITGA7):c.3150G>T (p.Leu1050=) rs114735704 0.00135
NM_002206.3(ITGA7):c.1008C>T (p.Asp336=) rs145114073 0.00090
NM_002206.3(ITGA7):c.791-7C>T rs144699549 0.00087
NM_002206.3(ITGA7):c.1606C>T (p.Leu536Phe) rs149028067 0.00083
NM_002206.3(ITGA7):c.1659C>G (p.Pro553=) rs144052152 0.00075
NM_002206.3(ITGA7):c.1828G>A (p.Gly610Arg) rs150583010 0.00071
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.999-4A>G rs370741662 0.00033
NM_002206.3(ITGA7):c.1765A>C (p.Ile589Leu) rs200065922 0.00032
NM_002206.3(ITGA7):c.2710C>T (p.Leu904=) rs200149396 0.00031
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.1410-3del rs773251917
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.671-5C>A rs180841797
NM_002206.3(ITGA7):c.708C>A (p.Pro236=) rs555521550

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