List of variants in gene BRIP1 reported as uncertain significance by MGZ Medical Genetics Center

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_032043.3(BRIP1):c.3444C>A (p.Asp1148Glu)	rs28997573	0.00011
NM_032043.3(BRIP1):c.1619A>T (p.Gln540Leu)	rs4988349	0.00003
NM_032043.3(BRIP1):c.728T>C (p.Ile243Thr)	rs587781860	0.00003
NM_032043.3(BRIP1):c.326A>G (p.Asn109Ser)	rs587782734	0.00001
NM_032043.3(BRIP1):c.823A>G (p.Ile275Val)	rs587781425	0.00001
NM_032043.3(BRIP1):c.1336A>T (p.Ile446Phe)
NM_032043.3(BRIP1):c.2710G>A (p.Asp904Asn)	rs1555573413
NM_032043.3(BRIP1):c.626A>G (p.Lys209Arg)	rs748912293
NM_032043.3(BRIP1):c.93+5G>A	rs730881629
NM_032043.3(BRIP1):c.983T>C (p.Phe328Ser)	rs876659057

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