ClinVar Miner

List of variants in gene combination FANCD2, FANCD2OS reported as likely benign for abdominal and pelvic region disorder

Included ClinVar conditions (913):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 5
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HGVS dbSNP
NM_001018115.2(FANCD2):c.4281+270A>G rs17032386
NM_033084.5(FANCD2):c.3165C>T (p.Tyr1055=) rs375929975
NM_033084.5(FANCD2):c.3645T>A (p.Pro1215=) rs1168183069
NM_033084.5(FANCD2):c.4362G>A (p.Leu1454=) rs145889419
NM_033084.5(FANCD2):c.4396C>A (p.Pro1466Thr) rs78896323

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