List of variants reported as pathogenic for pregnancy disorder by Medical Genetics Laboratory, CHRU Nancy

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
GRCh37/hg19 17q12(chr17:34437475-36243028)
GRCh37/hg19 2q11.1-11.2(chr2:96755045-98021592)
GRCh37/hg19 4p16.3(chr4:388344-3872380)

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