ClinVar Miner

List of variants in gene SNX17, ZNF513 studied for retinal disorder

Included ClinVar conditions (500):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 12
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HGVS dbSNP gnomAD frequency
NM_144631.6(ZNF513):c.*173C>T rs13472 0.37643
NM_144631.6(ZNF513):c.*29C>T rs148848066 0.00062
NM_144631.6(ZNF513):c.*129G>A rs560324766 0.00051
NM_144631.6(ZNF513):c.*134A>G rs754539683 0.00028
NM_144631.6(ZNF513):c.*174G>A rs558608689 0.00021
NM_144631.6(ZNF513):c.*15C>T rs377145066 0.00017
NM_144631.6(ZNF513):c.*54C>T rs149692692 0.00014
NM_144631.6(ZNF513):c.*225G>A rs575633762 0.00013
NM_144631.6(ZNF513):c.*60C>T rs753288919 0.00013
NM_144631.6(ZNF513):c.*254T>A rs916987949 0.00001
NM_144631.6(ZNF513):c.*164G>A rs1004503387
NM_144631.6(ZNF513):c.*217G>C rs536704518

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