Hi,
I have a PhD + experience in human genetics.
I worked with sequencing data to find causative variants.
I will need the available data (BAM, VCF files, ...) + information about the Exome library that is use in the test if available.
And the data should be compressed with a password to be able to get it through internet based on the EU data protection rules.
I offer here to give you:
1- List of all SNPs in exons with their genotypes.
2- Annotate the VCF file with annotations that important for clinical purpose with the frequency of each variant in the population.
3- After the annotation step, I offer a filtering step if you want to get the list of filtered variants to avoid the false positives and to get the most important variants.