List of variants in gene INF2 reported by OMIM

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_022489.4(INF2):c.641G>A (p.Arg214His)	rs267606879	0.00001
NM_022489.4(INF2):c.125T>C (p.Leu42Pro)	rs267606880
NM_022489.4(INF2):c.310T>C (p.Cys104Arg)	rs387907034
NM_022489.4(INF2):c.311G>T (p.Cys104Phe)	rs387907035
NM_022489.4(INF2):c.312C>G (p.Cys104Trp)	rs387907036
NM_022489.4(INF2):c.383T>C (p.Leu128Pro)	rs387907037
NM_022489.4(INF2):c.395T>G (p.Leu132Arg)	rs387907038
NM_022489.4(INF2):c.490_498del (p.Ala164_Asp166del)	rs1555373599
NM_022489.4(INF2):c.556T>C (p.Ser186Pro)	rs267606877
NM_022489.4(INF2):c.652C>T (p.Arg218Trp)	rs267606878
NM_022489.4(INF2):c.653G>A (p.Arg218Gln)	rs267607183

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