ClinVar Miner

List of variants in gene ITGA7 reported as likely benign for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 60
Download table as spreadsheet
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.459C>G (p.Ile153Met) rs149000088 0.00672
NM_002206.3(ITGA7):c.2959-85A>G rs116101967 0.00662
NM_002206.3(ITGA7):c.1609C>T (p.Arg537Trp) rs61733050 0.00636
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.2644G>A (p.Glu882Lys) rs144983062 0.00347
NM_002206.3(ITGA7):c.2003+267G>C rs138357077 0.00319
NM_002206.3(ITGA7):c.2701A>G (p.Ile901Val) rs113651939 0.00295
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.2737C>T (p.Arg913Trp) rs140030984 0.00169
NM_002206.3(ITGA7):c.610G>A (p.Ala204Thr) rs76770808 0.00146
NM_002206.3(ITGA7):c.139G>A (p.Glu47Lys) rs77929806 0.00088
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.537G>A (p.Gly179=) rs145463677 0.00061
NM_002206.3(ITGA7):c.799A>G (p.Ile267Val) rs201469044 0.00025
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.3174C>T (p.Leu1058=) rs377148751 0.00006
NM_002206.3(ITGA7):c.63C>G (p.Ser21=) rs368615107 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.1197T>C (p.Ile399=) rs777273056 0.00001
NM_002206.3(ITGA7):c.2779C>T (p.Arg927Trp) rs760407686 0.00001
NM_002206.3(ITGA7):c.558A>G (p.Gly186=) rs552091036 0.00001
NM_002206.3(ITGA7):c.1410-3del rs773251917
NM_002206.3(ITGA7):c.1455A>G (p.Pro485=) rs1592447862
NM_002206.3(ITGA7):c.1505+86G>A rs80032534
NM_002206.3(ITGA7):c.207-263GT[15] rs57311080
NM_002206.3(ITGA7):c.2976G>A (p.Lys992=) rs1592403571
NM_002206.3(ITGA7):c.414+38GT[10] rs138614852
NM_002206.3(ITGA7):c.415-123CATGTG[4] rs373790389
NM_002206.3(ITGA7):c.63C>T (p.Ser21=) rs368615107
NM_002206.3(ITGA7):c.671-295G>A
NM_002206.3(ITGA7):c.671-5C>A rs180841797
NM_002206.3(ITGA7):c.738T>C (p.Pro246=) rs1592460865
NM_002206.3(ITGA7):c.762C>T (p.Ala254=) rs376003902

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.