ClinVar Miner

List of variants in gene ITGA2 reported by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 75
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_002203.4(ITGA2):c.295+176= rs27956 0.99998
NM_002203.4(ITGA2):c.1173+172A>T rs996765 0.88782
NM_002203.4(ITGA2):c.2236-102A>T rs2287872 0.88759
NM_002203.4(ITGA2):c.1806+274A>G rs2406599 0.88129
NM_002203.4(ITGA2):c.630+10A>G rs1421933 0.74623
NM_002203.4(ITGA2):c.64+305G>C rs40118 0.74456
NM_002203.4(ITGA2):c.2235+48G>A rs2112290 0.73868
NM_002203.4(ITGA2):c.2572-41G>A rs3212591 0.48379
NM_002203.4(ITGA2):c.2825+236C>T rs12518279 0.48073
NM_002203.4(ITGA2):c.931-68G>A rs3212522 0.47946
NM_002203.4(ITGA2):c.1097-242A>G rs1421929 0.47911
NM_002203.4(ITGA2):c.780-126A>G rs2974987 0.47731
NM_002203.4(ITGA2):c.630+237C>T rs2974978 0.47724
NM_002203.4(ITGA2):c.3145-151G>A rs2303123 0.45854
NM_002203.4(ITGA2):c.825G>A (p.Thr275=) rs1062535 0.37202
NM_002203.4(ITGA2):c.1312+12T>C rs2303127 0.36561
NM_002203.4(ITGA2):c.759C>T (p.Phe253=) rs1126643 0.36485
NM_002203.4(ITGA2):c.3252C>T (p.Phe1084=) rs2303122 0.34753
NM_002203.4(ITGA2):c.185+23G>T rs26678 0.27897
NM_002203.4(ITGA2):c.388-147G>A rs3212486 0.27510
NM_002203.4(ITGA2):c.387+142A>G rs1421937 0.27496
NM_002203.4(ITGA2):c.186-186A>G rs3212438 0.27457
NM_002203.4(ITGA2):c.186-34C>T rs3212441 0.27359
NM_002203.4(ITGA2):c.387+188T>G rs3212461 0.27352
NM_002203.4(ITGA2):c.295+32T>G rs1363192 0.27351
NM_002203.4(ITGA2):c.295+225T>C rs1316250 0.27345
NM_002203.4(ITGA2):c.186-159T>C rs3212439 0.27341
NM_002203.4(ITGA2):c.388-292C>T rs3212483 0.24737
NM_002203.4(ITGA2):c.3145-214G>A rs2303124 0.20328
NM_002203.4(ITGA2):c.1944-183A>T rs3212556 0.19174
NM_002203.4(ITGA2):c.1312+164C>T rs3212537 0.19111
NM_002203.4(ITGA2):c.2376C>T (p.Asp792=) rs3212583 0.12027
NM_002203.4(ITGA2):c.1174-138A>G rs3212536 0.11411
NM_002203.4(ITGA2):c.2235+291A>G rs3212569 0.11398
NM_002203.4(ITGA2):c.2484G>A (p.Thr828=) rs3212327 0.11398
NM_002203.4(ITGA2):c.2571+104A>G rs3815755 0.11388
NM_002203.4(ITGA2):c.2665-159G>T rs3212593 0.11338
NM_002203.4(ITGA2):c.2429+21T>C rs3212584 0.11329
NM_002203.4(ITGA2):c.2929-222G>A rs3212613 0.11326
NM_002203.4(ITGA2):c.1600G>A (p.Glu534Lys) rs1801106 0.11302
NM_002203.4(ITGA2):c.2235+194G>A rs3212567 0.11189
NM_002203.4(ITGA2):c.2236-53T>C rs3212580 0.11172
NM_002203.4(ITGA2):c.2236-219T>C rs2287873 0.11168
NM_002203.4(ITGA2):c.2571+246A>G rs3797474 0.11167
NM_002203.4(ITGA2):c.2347-77A>C rs3212582 0.11157
NM_002203.4(ITGA2):c.3466-118C>T rs875657 0.11152
NM_002203.4(ITGA2):c.2568G>A (p.Leu856=) rs3213805 0.11016
NM_002203.4(ITGA2):c.3259-127T>C rs3212634 0.10529
NM_002203.4(ITGA2):c.3259-34A>T rs3212635 0.08435
NM_002203.4(ITGA2):c.2235+72G>A rs2303126 0.07438
NM_002203.4(ITGA2):c.780-186A>G rs3212519 0.06538
NM_002203.4(ITGA2):c.65-209G>A rs3212666 0.05690
NM_002203.4(ITGA2):c.1174-188G>A rs3212684 0.05082
NM_002203.3(ITGA2):c.-124G>A rs3212385 0.04997
NM_002203.4(ITGA2):c.780-132C>T rs2910962 0.03890
NM_002203.4(ITGA2):c.3040-241T>A rs3212617 0.03686
NM_002203.4(ITGA2):c.2346+78G>T rs3212581 0.03422
NM_002203.4(ITGA2):c.1313-39T>C rs3212538 0.03237
NM_002203.4(ITGA2):c.85G>A (p.Ala29Thr) rs374701439 0.00003
NM_002203.4(ITGA2):c.1313-30T>G rs3212539
NM_002203.4(ITGA2):c.185+287_185+290dup rs3212422
NM_002203.4(ITGA2):c.2235+246T>C rs3212568
NM_002203.4(ITGA2):c.2236-62T>C rs2287871
NM_002203.4(ITGA2):c.2429+69C>T rs3212586
NM_002203.4(ITGA2):c.2430-26T>A rs984966
NM_002203.4(ITGA2):c.2664+125G>C rs2303125
NM_002203.4(ITGA2):c.295+190G>A rs2287950
NM_002203.4(ITGA2):c.3145-313del rs3212625
NM_002203.4(ITGA2):c.3348+54C>T rs2303120
NM_002203.4(ITGA2):c.630+180G>A rs3212487
NM_002203.4(ITGA2):c.630+257_630+258del rs111756330
NM_002203.4(ITGA2):c.64+283CA[12] rs35389760
NM_002203.4(ITGA2):c.64+283CA[13] rs35389760
NM_002203.4(ITGA2):c.64+309_64+312del rs756852335
NM_002203.4(ITGA2):c.779+172G>A rs1833558

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.