Update source4.csv

source4.csv

@@ -106,7 +106,7 @@ We both are silent carriers of it, since we both carry it there is a 1 in 4 chan
 However if he has a super rare form of it there are 25 cases in the entire world that baby with this has neurological issues (seizures, intellectual disabilities, autistic behavior). This is the part that is scary to me.
 My question is if anyone has seen this IRL or knows any research done on the neurological symptoms."
 Reddit,/r/GeneticCounseling,"I had a WES panel done with Prevention genetics due to a high NT in my baby at 13 weeks pregnant. My doctor told me they ran only primary findings and issues associated with high NT. I’m not sure what that means or what the WES would cover then than the karyotype and microarray didn’t. Does anybody know? If you’ve had WES, how do you know what the test is looking for?"
-Reddit,/r/genetics,"Can someone smarter than me help break this down? My husband and I are waiting for results of our genetic testing. My husbands brother is a carrier of a cystic fibrosis gene. We are operating under the assumption he may have the gene as well.
+Reddit,/r/genetics,"My husband and I are waiting for results of our genetic testing. My husbands brother is a carrier of a cystic fibrosis gene. We are operating under the assumption he may have the gene as well.
 We have dna reports from both of my parents. My dad's report was flagged by genetic genie for the following gene:
 variant:c.3897A>g rsid:rs1800131
 My reading is telling me that variant is benign so my questions are - should I be prepared to be flagged as a carrier if I also have that \"benign\" gene? And will it impact our future children if I have a benign gene but my husband has one of the more typical carrying genes."