ClinVar Miner

List of variants in gene CFHR5 reported as likely benign for abdominal and pelvic region disorder

Included ClinVar conditions (956):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 7
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HGVS dbSNP
NM_030787.3(CFHR5):c.*397C>G rs115744316
NM_030787.3(CFHR5):c.243G>A (p.Pro81=) rs7532068
NM_030787.3(CFHR5):c.254-8T>G rs114023763
NM_030787.3(CFHR5):c.330A>C (p.Val110=) rs61745675
NM_030787.3(CFHR5):c.434G>A (p.Gly145Glu) rs57960694
NM_030787.3(CFHR5):c.485_486dup (p.Glu163fs) rs565457964
NM_030787.3(CFHR5):c.507C>T (p.Asp169=) rs34533956

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