ClinVar Miner

List of variants in gene combination AOPEP, FANCC reported as likely pathogenic by Invitae

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 6
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HGVS dbSNP
NM_000136.2(FANCC):c.1329+1G>T rs1554829441
NM_000136.2(FANCC):c.843+1G>A rs587779909
NM_000136.2(FANCC):c.844-1G>C rs774209201
NM_000136.2(FANCC):c.896+1G>C rs1554833186
NM_000136.2(FANCC):c.896+2T>G rs863224441
NM_000136.2(FANCC):c.996+1G>T rs370510954

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