Genome/Exome Data Interpretation (bioinformatics)

We are a genetic testing laboratory working with a human exome for the first time. We need help analysing the data. We will provide the exome files for analysis. It would be great if you could take this data and help us find clinically relevant variations. The person is thought to be generally healthy. The job includes: 1) Analyse Exome data (Bam files, fastaqc, bai, vcf available) for one humen exome. We need info such as clinically relevant mutations, carrier status etc. 2) The VCF gives us variatons that differ from the reference sequence only. We do however also need info which SNPs are wildtype. Give us a list of SNP rs numbers that were covered by the Exome (Not just the ones that differ from the reference data). Please DO NOT bid if you dont know what a BAM file or reference genome is. Many follow up projects are likely if things go well!