List of variants in gene ITGB2 reported by Genomic Research Center, Shahid Beheshti University of Medical Sciences

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: 25

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HGVS	dbSNP	gnomAD frequency
NM_000211.5(ITGB2):c.1062= (p.His354=)	rs235330	0.99991
NM_000211.5(ITGB2):c.994-47G>A	rs2838725	0.24547
NM_000211.5(ITGB2):c.1101C>A (p.Val367=)	rs2230529	0.23426
NM_000211.5(ITGB2):c.2248-127G>C	rs235375	0.22047
NM_000211.5(ITGB2):c.819G>A (p.Gly273=)	rs2230528	0.21986
NM_000211.5(ITGB2):c.24G>T (p.Leu8=)	rs11088969	0.20978
NM_000211.5(ITGB2):c.500-11G>T	rs55865320	0.16920
NM_000211.5(ITGB2):c.742-13G>A	rs5030670	0.12263
NM_000211.5(ITGB2):c.58+12G>A	rs2280965	0.09186
NM_000211.5(ITGB2):c.329-6C>T	rs9983887	0.00876
NM_000211.5(ITGB2):c.381C>T (p.Ile127=)	rs483352812	0.00007
NM_000211.5(ITGB2):c.897+1G>A	rs201752283	0.00004
NM_000211.4(ITGB2):c.[576dupC];[706G>A]
NM_000211.5(ITGB2):c.1030G>T (p.Glu344Ter)	rs483352816
NM_000211.5(ITGB2):c.1143del (p.Tyr382fs)	rs483352817
NM_000211.5(ITGB2):c.1877+2T>C	rs483352818
NM_000211.5(ITGB2):c.1878-45dup	rs35293792
NM_000211.5(ITGB2):c.1907del (p.Lys636fs)	rs483352819
NM_000211.5(ITGB2):c.2247+57C>T	rs33973568
NM_000211.5(ITGB2):c.382G>T (p.Asp128Tyr)	rs137852615
NM_000211.5(ITGB2):c.576dup (p.Asn193fs)	rs483352813
NM_000211.5(ITGB2):c.706G>A (p.Gly236Arg)	rs483352814
NM_000211.5(ITGB2):c.715G>A (p.Ala239Thr)	rs179363873
NM_000211.5(ITGB2):c.843del (p.Asn282fs)	rs483352815
NM_000211.5(ITGB2):c.897+1G>T	rs201752283

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