List of variants in gene ITGA2B reported by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_000419.5(ITGA2B):c.439C>G (p.Leu147Val)	rs76066357	0.00936
NM_000419.5(ITGA2B):c.2916G>A (p.Pro972=)	rs5913	0.00354
NM_000419.5(ITGA2B):c.2602G>A (p.Val868Met)	rs74988902	0.00239
NM_000419.5(ITGA2B):c.2965G>A (p.Ala989Thr)	rs78165611	0.00065
NM_000419.5(ITGA2B):c.457G>A (p.Ala153Thr)	rs199641871	0.00014
NM_000419.5(ITGA2B):c.2198C>T (p.Ala733Val)	rs201042087	0.00008
NM_000419.5(ITGA2B):c.1375G>A (p.Asp459Asn)
NM_000419.5(ITGA2B):c.1666G>T (p.Gly556Cys)
NM_000419.5(ITGA2B):c.188+8G>A	rs13306471
NM_000419.5(ITGA2B):c.1880C>A (p.Thr627Lys)
NM_000419.5(ITGA2B):c.1882C>T (p.Arg628Ter)	rs1236922680
NM_000419.5(ITGA2B):c.2010C>A (p.Asn670Lys)
NM_000419.5(ITGA2B):c.2094+7C>T
NM_000419.5(ITGA2B):c.2602-4C>G
NM_000419.5(ITGA2B):c.2993G>T (p.Trp998Leu)

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