ClinVar Miner

List of variants in gene combination LOC128706665, LOC128706666, MKKS reported as benign for autosomal recessive disease

Included ClinVar conditions (1198):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 2
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HGVS dbSNP gnomAD frequency
NM_170784.3(MKKS):c.-618C>T rs146473397 0.00078
NM_001394148.2(LOC128706665):c.-56_-47dup rs16996729

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