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NM_000249.3(MLH1):c.1668-19A>G AND Hereditary cancer-predisposing syndrome

Significance: Benign
ClinVar: RCV000447202

Variant: NM_000249.3(MLH1):c.1668-19A>G

Type: Variant
Allele: NM_000249.3(MLH1):c.1668-19A>G 45204
Gene:
Type: single nucleotide variant
Location: Chr3: 37083740 - assembly GRCh37
Chr3: 37042249 - assembly GRCh38
References: dbSNP: 9876116
International Society for Gastrointestinal Hereditary Tumours (InSiGHT): c.1668-19A>G

Condition

Disease: Hereditary cancer-predisposing syndrome