ClinVar Miner

List of variants in gene ITGA7 reported as uncertain significance for not provided

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Gene type:
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Total variants: 67
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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.2651A>T (p.Glu884Val) rs149963176 0.00081
NM_002206.3(ITGA7):c.3203C>T (p.Ala1068Val) rs139136931 0.00073
NM_002206.3(ITGA7):c.1722C>A (p.Ala574=) rs142311782 0.00066
NM_002206.3(ITGA7):c.340A>G (p.Met114Val) rs146565340 0.00063
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.671G>C (p.Gly224Ala) rs537950420 0.00033
NM_002206.3(ITGA7):c.1765A>C (p.Ile589Leu) rs200065922 0.00032
NM_002206.3(ITGA7):c.1681G>A (p.Val561Met) rs150089409 0.00029
NM_002206.3(ITGA7):c.3268C>T (p.Gln1090Ter) rs200390529 0.00025
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.1807C>T (p.Arg603Trp) rs375836925 0.00013
NM_002206.3(ITGA7):c.517C>T (p.Arg173Trp) rs368130279 0.00013
NM_002206.3(ITGA7):c.3002A>T (p.Asn1001Ile) rs201796615 0.00012
NM_002206.3(ITGA7):c.1589C>T (p.Ala530Val) rs200267194 0.00011
NM_002206.3(ITGA7):c.3200G>A (p.Arg1067Gln) rs752159189 0.00008
NM_002206.3(ITGA7):c.1624C>T (p.Arg542Cys) rs374384926 0.00007
NM_002206.3(ITGA7):c.1625G>A (p.Arg542His) rs17854598 0.00007
NM_002206.3(ITGA7):c.3299T>C (p.Leu1100Pro) rs370654924 0.00006
NM_002206.3(ITGA7):c.1568-9A>G rs761067098 0.00005
NM_002206.3(ITGA7):c.259C>T (p.Arg87Cys) rs140570573 0.00005
NM_002206.3(ITGA7):c.1829G>T (p.Gly610Val) rs550384423 0.00004
NM_002206.3(ITGA7):c.2545C>G (p.Gln849Glu) rs143055936 0.00004
NM_002206.3(ITGA7):c.260G>A (p.Arg87His) rs775800333 0.00004
NM_002206.3(ITGA7):c.287T>G (p.Leu96Trp) rs886042999 0.00004
NM_002206.3(ITGA7):c.2963A>G (p.Tyr988Cys) rs1191095890 0.00004
NM_002206.3(ITGA7):c.3309C>G (p.Asn1103Lys) rs768823556 0.00003
NM_002206.3(ITGA7):c.104A>G (p.Asn35Ser) rs765097884 0.00002
NM_002206.3(ITGA7):c.1273C>T (p.Pro425Ser) rs886727586 0.00002
NM_002206.3(ITGA7):c.1982C>T (p.Thr661Met) rs749679578 0.00002
NM_002206.3(ITGA7):c.2740C>T (p.Arg914Trp) rs754109651 0.00002
NM_002206.3(ITGA7):c.518G>A (p.Arg173Gln) rs144639829 0.00002
NM_002206.3(ITGA7):c.571C>T (p.His191Tyr) rs984817118 0.00002
NM_002206.3(ITGA7):c.671-306C>T rs754813765 0.00002
NM_002206.3(ITGA7):c.1244A>G (p.His415Arg) rs1355871507 0.00001
NM_002206.3(ITGA7):c.1283T>C (p.Val428Ala) rs201554972 0.00001
NM_002206.3(ITGA7):c.128G>T (p.Arg43Leu) rs794726901 0.00001
NM_002206.3(ITGA7):c.157G>A (p.Gly53Ser) rs757119118 0.00001
NM_002206.3(ITGA7):c.1771G>A (p.Val591Met) rs774213412 0.00001
NM_002206.3(ITGA7):c.1969C>T (p.Arg657Trp) rs528020122 0.00001
NM_002206.3(ITGA7):c.205T>G (p.Trp69Gly) rs1875458381 0.00001
NM_002206.3(ITGA7):c.2779C>T (p.Arg927Trp) rs760407686 0.00001
NM_002206.3(ITGA7):c.2854C>T (p.Arg952Trp) rs758865138 0.00001
NM_002206.3(ITGA7):c.2908G>A (p.Ala970Thr) rs767472988 0.00001
NM_002206.3(ITGA7):c.3040C>T (p.Arg1014Ter) rs377510220 0.00001
NM_002206.3(ITGA7):c.3082C>T (p.Pro1028Ser) rs779998014 0.00001
NM_002206.3(ITGA7):c.3118G>T (p.Val1040Phe) rs764565180 0.00001
NM_002206.3(ITGA7):c.883G>C (p.Val295Leu) rs781541108 0.00001
NM_002206.3(ITGA7):c.1012A>G (p.Ile338Val) rs879008268
NM_002206.3(ITGA7):c.1040G>T (p.Arg347Leu) rs775063840
NM_002206.3(ITGA7):c.1854C>T (p.Leu618=) rs372612921
NM_002206.3(ITGA7):c.206+4A>T
NM_002206.3(ITGA7):c.2590A>G (p.Met864Val)
NM_002206.3(ITGA7):c.2642T>A (p.Val881Asp) rs794727321
NM_002206.3(ITGA7):c.3349A>C (p.Ile1117Leu) rs1482793424
NM_002206.3(ITGA7):c.467C>A (p.Thr156Lys) rs375671999
NM_002206.3(ITGA7):c.482G>T (p.Gly161Val) rs2136056460
NM_002206.3(ITGA7):c.656C>T (p.Thr219Ile) rs765610371
NM_002206.3(ITGA7):c.671-1G>A rs777049999
NM_002206.3(ITGA7):c.671-285A>G rs1873675449
NM_002206.3(ITGA7):c.671-401C>T
NM_002206.3(ITGA7):c.708C>A (p.Pro236=) rs555521550
NM_002206.3(ITGA7):c.976G>T (p.Val326Leu)

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