ClinVar Miner

List of intergenic variants reported as pathogenic for autosomal anomaly

Included ClinVar conditions (123):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 6
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HGVS dbSNP gnomAD frequency
46,XY,der(21)t(9;21)(p11;p12)
NC_000001.11:g.(146472798_148439081)dup rs2101549505
NC_000002.10:g.146798229_150310317del
NC_000002.12:g.(211789273_236710421)dup rs2106321147
NR_039729.1(MIR2392):n.-10132_-1575del
Single allele

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