Given a ClinVar Pathogenic SNP
rs35269064 (NM_000050.4(ASS1):c.[323G>T];[970+5G>A] – Compound heterozygote).
Link: https://www.ncbi.nlm.nih.gov/clinvar/variation/424822/
How do I identify the risk allele of this rsID?
Thank you in advance.
rs35269064 (NM_000050.4(ASS1):c.[323G>T];[970+5G>A] – Compound heterozygote).
Link: https://www.ncbi.nlm.nih.gov/clinvar/variation/424822/
How do I identify the risk allele of this rsID?
Thank you in advance.
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