ClinVar Miner

List of variants in gene ITGA7 reported as likely benign by GeneDx

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 68
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HGVS dbSNP gnomAD frequency
NM_002206.3(ITGA7):c.2958+56G>A rs117082867 0.01979
NM_002206.3(ITGA7):c.3183+244A>G rs139773973 0.01729
NM_002206.3(ITGA7):c.791-163G>C rs118129867 0.01423
NM_001144997.2(ITGA7):c.85+3855dup rs139802087 0.01413
NM_002206.3(ITGA7):c.414+222A>T rs141473012 0.01403
NM_002206.3(ITGA7):c.415-175C>T rs74569994 0.01397
NM_001144997.2(ITGA7):c.-12G>A rs7295335 0.01299
NM_002206.3(ITGA7):c.2845-319G>A rs114910004 0.01146
NM_002206.3(ITGA7):c.998+66C>A rs11171658 0.00945
NM_001144997.2(ITGA7):c.38C>T (p.Thr13Ile) rs11171663 0.00943
NM_002206.3(ITGA7):c.790+261G>A rs117793692 0.00875
NM_002206.3(ITGA7):c.1738-23G>A rs149716542 0.00717
NM_002206.3(ITGA7):c.2713-63G>T rs145346103 0.00704
NM_002206.3(ITGA7):c.1281+13G>A rs143895796 0.00701
NM_002206.3(ITGA7):c.2959-85A>G rs116101967 0.00662
NM_002206.3(ITGA7):c.3184-103C>T rs146570241 0.00621
NM_002206.3(ITGA7):c.671-130T>C rs139539572 0.00616
NM_001144997.2(ITGA7):c.-18G>T rs145243860 0.00591
NM_002206.3(ITGA7):c.1888-263C>T rs147238303 0.00535
NM_002206.3(ITGA7):c.3384C>T (p.Pro1128=) rs148170949 0.00509
NM_002206.3(ITGA7):c.2844+46C>T rs148775515 0.00382
NM_002206.3(ITGA7):c.1567+65G>C rs374530008 0.00366
NM_002206.3(ITGA7):c.1506-14C>T rs148374832 0.00322
NM_002206.3(ITGA7):c.2003+267G>C rs138357077 0.00319
NM_002206.3(ITGA7):c.2844+36C>T rs117488030 0.00288
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.2958+16G>A rs200586885 0.00207
NM_002206.3(ITGA7):c.610G>A (p.Ala204Thr) rs76770808 0.00146
NM_002206.3(ITGA7):c.3150G>T (p.Leu1050=) rs114735704 0.00135
NM_002206.3(ITGA7):c.139G>A (p.Glu47Lys) rs77929806 0.00088
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.2844+19C>T rs141542046 0.00026
NM_002206.3(ITGA7):c.799A>G (p.Ile267Val) rs201469044 0.00025
NM_002206.3(ITGA7):c.609C>T (p.Ala203=) rs140554289 0.00024
NM_002206.3(ITGA7):c.1023C>T (p.Ala341=) rs367953820 0.00020
NM_002206.3(ITGA7):c.1317C>T (p.Phe439=) rs200714716 0.00019
NM_002206.3(ITGA7):c.3363C>T (p.Asp1121=) rs372977210 0.00008
NM_002206.3(ITGA7):c.1266C>T (p.Val422=) rs1475493786 0.00006
NM_002206.3(ITGA7):c.2625G>A (p.Leu875=) rs370716816 0.00006
NM_002206.3(ITGA7):c.69C>T (p.Leu23=) rs146932796 0.00006
NM_002206.3(ITGA7):c.3372C>T (p.Pro1124=) rs141486781 0.00005
NM_002206.3(ITGA7):c.708C>T (p.Pro236=) rs555521550 0.00005
NM_002206.3(ITGA7):c.1568-18T>C rs371316432 0.00004
NM_002206.3(ITGA7):c.2556G>A (p.Ser852=) rs138301131 0.00003
NM_002206.3(ITGA7):c.-9G>A rs755539302 0.00001
NM_002206.3(ITGA7):c.1409+11C>T rs748472564 0.00001
NM_002206.3(ITGA7):c.3048C>T (p.Ala1016=) rs1312920904 0.00001
NM_002206.3(ITGA7):c.558A>G (p.Gly186=) rs552091036 0.00001
NM_002206.3(ITGA7):c.1263T>G (p.Val421=) rs1555162963
NM_002206.3(ITGA7):c.1410-3del rs773251917
NM_002206.3(ITGA7):c.1505+14G>C rs940004287
NM_002206.3(ITGA7):c.1505+86G>A rs80032534
NM_002206.3(ITGA7):c.1567+16C>G rs199504152
NM_002206.3(ITGA7):c.207-263GT[15] rs57311080
NM_002206.3(ITGA7):c.2628G>A (p.Leu876=) rs1555160400
NM_002206.3(ITGA7):c.2845-18G>A rs1555159028
NM_002206.3(ITGA7):c.2946C>T (p.Ser982=) rs1555158844
NM_002206.3(ITGA7):c.414+38GT[10] rs138614852
NM_002206.3(ITGA7):c.415-123CATGTG[4] rs373790389
NM_002206.3(ITGA7):c.671-5C>A rs180841797
NM_002206.3(ITGA7):c.810G>T (p.Gly270=) rs3847675

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