List of variants in gene CD36 reported as pathogenic for Platelet-type bleeding disorder 10

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

Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_001001548.3(CD36):c.975T>G (p.Tyr325Ter)	rs3211938	0.02669
NM_001001548.3(CD36):c.1079T>G (p.Leu360Ter)	rs56381858	0.00017
NM_001001548.3(CD36):c.268C>T (p.Pro90Ser)	rs75326924	0.00011
CD36, G1439C, 1-BP DEL, 1444A
NM_001001547.2(CD36):c.120+399TG[12]
NM_001001547.2:c.(?_-183)_(120_?)del
NM_001001548.3(CD36):c.1228_1239del (p.Ile410_Ile413del)	rs550565800
NM_001001548.3(CD36):c.1237A>C (p.Ile413Leu)	rs121918035
NM_001001548.3(CD36):c.1240_1243dup (p.Trp415fs)	rs757142781
NM_001001548.3(CD36):c.332_333del (p.Thr111fs)	rs572295823
NM_001001548.3(CD36):c.447_450dup (p.Asn151fs)	rs780114238
NM_001001548.3(CD36):c.638_639del (p.Lys213fs)	rs780525946
NM_001001548.3(CD36):c.667_671dup (p.Ala225fs)	rs748431584
NM_001001548.3(CD36):c.729C>A (p.Cys243Ter)	rs149985988
NM_001001548.3(CD36):c.760T>C (p.Phe254Leu)	rs142186404
NM_001001548.3(CD36):c.787_808del (p.Val263fs)	rs754365623
NM_001001548.3(CD36):c.949dup (p.Ile317fs)	rs70961716

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