List of variants reported as pathogenic for colorectal cancer by Department of Human Genetics, Hannover Medical School

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
GRCh38/hg38 2p21(chr2:47416275-47416449)x1
NM_000179.3(MSH6):c.3261del (p.Phe1088fs)	rs267608078
NM_000179.3(MSH6):c.4001G>A (p.Arg1334Gln)	rs267608122
NM_000249.4(MLH1):c.108dup (p.Glu37Ter)
NM_000249.4(MLH1):c.1871dup (p.Asp624fs)
NM_000251.3(MSH2):c.1428del (p.Asn477fs)	rs2104086603
NM_000251.3(MSH2):c.425C>A (p.Ser142Ter)	rs63750910

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