ClinVar Miner

List of variants reported by Clinical Genetics Branch, National Institutes of Health

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 5
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HGVS dbSNP gnomAD frequency
NR_002328.4:n.683T>C rs61746197 0.00503
NM_006060.6(IKZF1):c.1267C>T (p.Arg423Cys) rs757907717 0.00003
NC_000001.11:g.145601946_148597425del
NC_000007.14:g.66971410_66990307del
NM_016038.4(SBDS):c.258+347_459+223del rs2536928013

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