List of variants reported as likely pathogenic by Hereditary Cancer Genetics group, Vall d'Hebron Institute of Oncology

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_007294.4(BRCA1):c.4185+4105C>T	rs1597853155	0.00001
NM_007294.4(BRCA1):c.4484+5G>C	rs886040910
NM_007294.4(BRCA1):c.4675+1G>C	rs80358044
NM_007294.4(BRCA1):c.5333-3T>G	rs397509265
NM_007294.4(BRCA1):c.5468-1_5468delinsTT	rs1597797251
NM_024675.4(PALB2):c.3201+5G>T	rs1597073208

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