ClinVar Miner

List of variants in gene ITGA2, MOCS2 studied for hematologic disorder

Included ClinVar conditions (812):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 34
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HGVS dbSNP gnomAD frequency
NM_002203.4(ITGA2):c.*721A>C rs1109527 0.88662
NM_002203.4(ITGA2):c.*3026A>G rs7719848 0.75000
NM_002203.4(ITGA2):c.*894C>T rs1109526 0.74563
NM_002203.4(ITGA2):c.*3986A>C rs7725246 0.35845
NM_002203.4(ITGA2):c.*2940G>A rs6898333 0.34995
NM_002203.4(ITGA2):c.*2999A>G rs6880055 0.31005
NM_004531.5(MOCS2):c.*2158C>T rs17298242 0.20066
NM_004531.5(MOCS2):c.*413del rs3839261 0.15118
NM_004531.5(MOCS2):c.*1872C>T rs77227647 0.11611
NM_002203.4(ITGA2):c.*3918G>C rs10471829 0.11354
NM_002203.4(ITGA2):c.*2574C>G rs75427194 0.11349
NM_002203.4(ITGA2):c.*3164G>A rs7737412 0.11348
NM_002203.4(ITGA2):c.*1252G>A rs1042324 0.11343
NM_004531.5(MOCS2):c.*2032G>A rs75571463 0.11337
NM_004531.5(MOCS2):c.*2415C>T rs16880872 0.10619
NM_002203.4(ITGA2):c.*4098C>G rs10471830 0.10454
NM_002203.4(ITGA2):c.*2939C>T rs7700416 0.10451
NM_004531.5(MOCS2):c.*2582A>C rs12518145 0.00995
NM_004531.5(MOCS2):c.*321A>G rs73756618 0.00849
NM_004531.5(MOCS2):c.*1913G>A rs193054707 0.00676
NM_004531.5(MOCS2):c.*2045G>A rs577647122 0.00111
NM_004531.5(MOCS2):c.*171G>C rs191465075 0.00003
NM_002203.4(ITGA2):c.*1764del rs3212655
NM_002203.4(ITGA2):c.*2041del rs35863692
NM_002203.4(ITGA2):c.*2505CAAA[3] rs72277253
NM_002203.4(ITGA2):c.*2570C>A rs1900182
NM_002203.4(ITGA2):c.*2570C>T rs1900182
NM_002203.4(ITGA2):c.*3385_*3386insGAAA rs59915734
NM_002203.4(ITGA2):c.*3763_*3764del rs145759303
NM_002203.4(ITGA2):c.*3813G>A rs1740598174
NM_002203.4(ITGA2):c.*4045AGT[1] rs71727762
NM_002203.4(ITGA2):c.*475_*477del rs199677547
NM_002203.4(ITGA2):c.*760_*761insTTAT rs3212652
NM_004531.5(MOCS2):c.*44A>C rs367775935

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