ClinVar Miner

List of variants in gene LOC108281170, LOC108281180, NF1 studied for RASopathy

Included ClinVar conditions (83):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 3
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HGVS dbSNP gnomAD frequency
GRCh38/hg38 17q11.2(chr17:31155962-31163396)x1
NC_000017.11:g.(?_31155977)_(31163382_?)del
NM_001042492.3(NF1):c.205-1284_289-944del

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