One Pathogenic variant identified in MSH2. MSH2 is associated with autosomal dominant Lynch
syndrome and autosomal recessive constitutional mismatch repair deficiency syndrome.
Additional Variant(s) of Uncertain Significance identified.
GENE VARIANT ZYGOSITY VARIANT CLASSIFICATION
MSH2 c.998G>A (p.Cys333Tyr) heterozygous PATHOGENIC
WRN c.919A> T (p.Thr307Ser) heterozygous Uncertain Significance
Greetings In Christ.
I am a Father of two(2) daughters with an-ongoing chemotherapy treatment of 10 sessions out of 12 sessions because of colon-rectal cancer. The surgery was done last May 2020. Besides, I undergo genetic testing and the sample saliva was sent to Invitae in the U.S. The above-stated report resulted in a positive, MSH2. By God’s Grace, I ask for completed healing of these diseases and believe, it will heal in my generation and free our Children.
Amen.
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