ClinVar Miner

List of variants in gene CNNM2 studied for abdominal and pelvic region disorder

Included ClinVar conditions (902):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 5
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HGVS dbSNP
NM_017649.5(CNNM2):c.1069G>A (p.Glu357Lys) rs786205910
NM_017649.5(CNNM2):c.117del (p.Ile40fs) rs1564803221
NM_017649.5(CNNM2):c.1703C>T (p.Thr568Ile) rs387906975
NM_017649.5(CNNM2):c.364G>A (p.Glu122Lys) rs786205909
NM_017649.5(CNNM2):c.806C>G (p.Ser269Trp) rs794726858

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