List of variants in gene INF2 reported as benign for not provided

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Gene type:		Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 11

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HGVS	dbSNP
NM_001031714.3(INF2):c.1274C>T (p.Pro425Leu)	rs1555374270
NM_022489.3(INF2):c.1582C>T (p.Pro528Ser)	rs181694819
NM_022489.3(INF2):c.2310+8delA	rs3840006
NM_022489.3(INF2):c.2630G>A (p.Arg877Gln)	rs142678449
NM_022489.3(INF2):c.2640T>C (p.Asp880=)	rs10133301
NM_022489.3(INF2):c.3066T>C (p.Asp1022=)	rs4983535
NM_022489.3(INF2):c.3153C>T (p.Asp1051=)	rs117457867
NM_022489.3(INF2):c.3207A>G (p.Pro1069=)	rs1128840
NM_022489.3(INF2):c.3478G>A (p.Gly1160Ser)	rs9672065
NM_022489.3(INF2):c.391+6C>T	rs75115369
NM_022489.3(INF2):c.42G>A (p.Leu14=)	rs62638758

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