ClinVar Miner

List of variants in gene combination LOC111811965, NF1 reported as uncertain significance for Watson syndrome

Included ClinVar conditions (4):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 18
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NM_000267.3(NF1):c.-115T>C rs886052793
NM_000267.3(NF1):c.-148C>A rs886052792
NM_000267.3(NF1):c.-173C>G rs886052791
NM_000267.3(NF1):c.-209C>A rs886052790
NM_000267.3(NF1):c.-229C>G rs886052789
NM_000267.3(NF1):c.-237C>T rs878967255
NM_000267.3(NF1):c.-237dup rs886052788
NM_000267.3(NF1):c.-242dup rs886052787
NM_000267.3(NF1):c.-248_-247dup rs886052786
NM_000267.3(NF1):c.-249_-247dup rs886052786
NM_000267.3(NF1):c.-322G>A rs886052785
NM_000267.3(NF1):c.-73G>T rs886052795
NM_000267.3(NF1):c.-84C>T rs886052794

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