List of variants in gene combination ITGA2, MOCS2 reported as benign for blood platelet disease

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 28

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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.*1913G>A	rs193054707	0.00676
NM_004531.5(MOCS2):c.*2045G>A	rs577647122	0.00111
NM_002203.4(ITGA2):c.*2041del	rs35863692
NM_002203.4(ITGA2):c.*2505CAAA[3]	rs72277253
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.*4045AGT[1]	rs71727762
NM_002203.4(ITGA2):c.475_477del	rs199677547
NM_002203.4(ITGA2):c.760_761insTTAT	rs3212652

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