ClinVar Miner

Variants in gene ARID1B with conflicting interpretations "likely pathogenic" and "uncertain significance"

Submission 1 (likely pathogenic) minimum review status: Submission 1 (likely pathogenic) method:
Submission 2 (uncertain significance) minimum review status: Submission 2 (uncertain significance) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 2
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HGVS dbSNP gnomAD frequency
NM_001374828.1(ARID1B):c.3236-1G>A rs752642190 0.00001
NM_001374828.1(ARID1B):c.1789C>T (p.Gln597Ter) rs1779032666

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