ClinVar Miner

List of variants in gene combination LOC111811965, NF1 reported as likely benign for RASopathy

Included ClinVar conditions (55):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 5
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NM_000267.3(NF1):c.-22G>C rs556823296
NM_000267.3(NF1):c.36C>A (p.Ala12=) rs786203866
NM_000267.3(NF1):c.36C>T (p.Ala12=) rs786203866
NM_000267.3(NF1):c.48C>T (p.Arg16=) rs1315327163
NM_000267.3(NF1):c.6C>T (p.Ala2=) rs876660128

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