ClinVar Miner

List of variants in gene NPHS2 reported as uncertain significance 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: 21
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HGVS dbSNP
NM_014625.3(NPHS2):c.-26G>T rs144425595
NM_014625.3(NPHS2):c.148C>T (p.Arg50Trp) rs886045596
NM_014625.3(NPHS2):c.191_193TGG[1] (p.Val65del) rs1553316600
NM_014625.3(NPHS2):c.274+14A>G rs757829667
NM_014625.3(NPHS2):c.372C>G (p.Cys124Trp) rs139290621
NM_014625.3(NPHS2):c.413G>A (p.Arg138Gln) rs74315342
NM_014625.3(NPHS2):c.467dup (p.Leu156fs) rs528833893
NM_014625.3(NPHS2):c.483C>A (p.Thr161=) rs754520138
NM_014625.3(NPHS2):c.523C>T (p.Pro175Ser) rs1472510122
NM_014625.3(NPHS2):c.622G>A (p.Ala208Thr) rs200587413
NM_014625.3(NPHS2):c.631T>A (p.Ser211Thr) rs779736229
NM_014625.3(NPHS2):c.652G>A (p.Val218Met) rs753108670
NM_014625.3(NPHS2):c.671G>A (p.Arg224His) rs138545216
NM_014625.3(NPHS2):c.67_69del (p.Glu23del) rs1398961188
NM_014625.3(NPHS2):c.686G>A (p.Arg229Gln) rs61747728
NM_014625.3(NPHS2):c.695C>T (p.Thr232Ile) rs774199987
NM_014625.3(NPHS2):c.724G>A (p.Ala242Thr) rs201355305
NM_014625.3(NPHS2):c.7_9AGG[1] (p.Arg4del) rs1553316672
NM_014625.3(NPHS2):c.85G>A (p.Ala29Thr) rs561887984
NM_014625.3(NPHS2):c.87C>G (p.Ala29=) rs12123397
NM_014625.3(NPHS2):c.88G>A (p.Glu30Lys) rs1477180313

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