parse clinvar xml by annovar

[asmlgkj]

thanks a lot for this excellent tool
due to the frequent update of clinvar, and vcf contains too little few info, for example, variant id(not allele id) and pmid, though there was separately files contains such, so does annovar can parse clinvar xlm?

[kaichop]

It does not process XLM file. But there was a recent update clinvar_20220320 that you can use. I am not sure what is a variant ID, in general the best way to identify a variant is the chr and position, not an ID. Most variants in clinvar has no PMID, since they are direct submissions.

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On Tue, Apr 26, 2022 at 5:31 AM curry_fan ***@***.***> wrote: thanks a lot for this excellent tool due to the frequent update of clinvar, and vcf contains too little few info, for example, variant id(not allele id) and pmid, though there was separately files contains such, so does annovar can parse clinvar xlm? — Reply to this email directly, view it on GitHub <#189>, or unsubscribe <https://github.com/notifications/unsubscribe-auth/ABNG3OB2HK4SBFIE6Z6YY3TVG6ZYTANCNFSM5ULGZI6A> . You are receiving this because you are subscribed to this thread.Message ID: ***@***.***>

[asmlgkj]

it was here variant ID, I have found a file about that, thanks a lot