ClinVar Miner

List of variants in gene NPHS2 reported as benign for abdominal and pelvic region disorder

Included ClinVar conditions (961):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 6
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NM_014625.3(NPHS2):c.-51G>T rs12406197
NM_014625.3(NPHS2):c.-52C>G rs78541594
NM_014625.3(NPHS2):c.102A>G (p.Gly34=) rs1079292
NM_014625.3(NPHS2):c.288C>T (p.Ser96=) rs3738423
NM_014625.3(NPHS2):c.59C>T (p.Pro20Leu) rs74315344
NM_014625.3(NPHS2):c.725C>T (p.Ala242Val) rs61747727

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