ClinVar Miner

List of variants in gene combination LOC129992166, WFS1 reported as likely benign by Clinical Genomics, Uppaluri K&H Personalized Medicine Clinic

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_006005.3(WFS1):c.-148G>T	rs542977017	0.00057
NM_006005.3(WFS1):c.-133G>T	rs886059521	0.00003

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