ClinVar Miner

List of variants in gene LOC105374344, RNF212 studied for chromosomal disorder

Included ClinVar conditions (200):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 1
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HGVS dbSNP gnomAD frequency
NR_134676.1(LOC105374344):n.52T>C rs62296477 0.61416

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