List of variants reported as benign for MHC class II deficiency by Natera, Inc.

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Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 30

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HGVS	dbSNP	gnomAD frequency
NM_000246.4(CIITA):c.2699A>G (p.Gln900Arg)	rs7197779	0.92908
NM_000246.4(CIITA):c.2676G>A (p.Thr892=)	rs2228238	0.64681
NM_000246.4(CIITA):c.1499G>C (p.Gly500Ala)	rs4774	0.27935
NM_000246.4(CIITA):c.2421G>T (p.Leu807=)	rs34654419	0.21279
NM_000246.4(CIITA):c.2394G>A (p.Pro798=)	rs2229320	0.16037
NM_000246.4(CIITA):c.3171C>T (p.Cys1057=)	rs2229322	0.09639
NM_000246.4(CIITA):c.2331G>T (p.Ser777=)	rs34685848	0.06730
NM_000246.4(CIITA):c.133C>G (p.Leu45Val)	rs2229317	0.06359
NM_000246.4(CIITA):c.2345T>C (p.Val782Ala)	rs13336804	0.06290
NM_000246.4(CIITA):c.2565G>A (p.Ala855=)	rs2229321	0.06266
NM_000246.4(CIITA):c.2342C>T (p.Ser781Leu)	rs13330686	0.06264
NM_000246.4(CIITA):c.225C>T (p.Cys75=)	rs2229318	0.03257
NM_000246.4(CIITA):c.2472C>T (p.His824=)	rs45621432	0.02015
NM_000246.4(CIITA):c.2072C>A (p.Ala691Asp)	rs78108426	0.01496
NM_000246.4(CIITA):c.2286C>A (p.Ile762=)	rs35976871	0.01268
NM_000246.4(CIITA):c.3255G>A (p.Thr1085=)	rs75521576	0.00964
NM_000246.4(CIITA):c.1973C>G (p.Ala658Gly)	rs2229319	0.00945
NM_000246.4(CIITA):c.200-10T>C	rs45474796	0.00588
NM_000246.4(CIITA):c.3108C>T (p.Ala1036=)	rs150276623	0.00215
NM_000246.4(CIITA):c.1461C>G (p.Ile487Met)	rs141202424	0.00124
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.1518G>A (p.Ala506=)	rs201215476	0.00043
NM_000246.4(CIITA):c.1926C>T (p.Val642=)	rs138376967	0.00033
NM_000246.4(CIITA):c.1047T>C (p.Tyr349=)	rs144735718	0.00014
NM_000246.4(CIITA):c.772+8C>T	rs557455283	0.00012
NM_000246.4(CIITA):c.2924A>G (p.Lys975Arg)	rs140103491	0.00011
NM_000246.4(CIITA):c.1486C>T (p.Leu496Phe)	rs756970534	0.00008
NM_000246.4(CIITA):c.3233+8_3233+9del	rs774399663
NM_000246.4(CIITA):c.494C>G (p.Thr165Ser)	rs34648899

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