List of variants in gene combination LOC129992166, WFS1 reported as benign for Wolfram syndrome

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_006005.3(WFS1):c.-130C>T	rs576284630	0.00207
NM_006005.3(WFS1):c.-141A>G	rs373287522	0.00036
NM_006005.3(WFS1):c.-129A>G	rs886059522	0.00013
NM_006005.3(WFS1):c.-105T>G	rs886059523	0.00011
NM_006005.3(WFS1):c.-106A>G	rs868329184	0.00003
NM_006005.3(WFS1):c.-100C>T	rs886059524
NM_006005.3(WFS1):c.-127A>G	rs542116747
NM_006005.3(WFS1):c.-93G>C	rs1729749153

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