List of variants in gene LOC130065872, MAFB studied for bone disorder

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_005461.5(MAFB):c.-310G>A	rs567415398	0.00147
NM_005461.5(MAFB):c.-297G>T	rs906559486	0.00028
NM_005461.5(MAFB):c.-269G>C	rs1986918651	0.00001

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