List of variants in gene CIITA reported as likely benign for not provided

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_000246.4(CIITA):c.*103T>C	rs45617532	0.00711
NM_000246.4(CIITA):c.2448C>T (p.Ala816=)	rs112250421	0.00272
NM_000246.4(CIITA):c.3108C>T (p.Ala1036=)	rs150276623	0.00215
NM_000246.4(CIITA):c.460G>A (p.Asp154Asn)	rs76923280	0.00106
NM_000246.4(CIITA):c.1068G>A (p.Pro356=)	rs140486686	0.00080
NM_000246.4(CIITA):c.691C>T (p.Pro231Ser)	rs147472574	0.00071
NM_000246.4(CIITA):c.2682G>A (p.Ala894=)	rs148091568	0.00064
NM_000246.4(CIITA):c.3153G>A (p.Leu1051=)	rs143507445	0.00004

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