ClinVar Miner

List of variants in gene combination LOC108281110, PAX8 reported as uncertain significance for hypothyroidism, congenital, nongoitrous

Included ClinVar conditions (10):

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)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_003466.4(PAX8):c.-63C>A	rs866836744	0.00023
NM_003466.4(PAX8):c.-75-4G>T	rs1693988335

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