List of variants in gene FANCB reported as likely benign for X-linked disease

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001018113.3(FANCB):c.2166-176A>G	rs6527026	0.99693
NM_001018113.3(FANCB):c.2166-186T>C	rs6527027	0.98887
NM_001018113.3(FANCB):c.951+129A>C	rs2375729	0.63356
NM_001018113.3(FANCB):c.-173G>C	rs2188383	0.63320
NM_001018113.3(FANCB):c.-70-246C>T	rs5935816	0.55158
NM_001018113.3(FANCB):c.1327-10T>C	rs2905223	0.53797

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