List of variants in gene CUL7, LOC129996487 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_014780.5(CUL7):c.-168C>T	rs3737186	0.09184
NM_014780.4(CUL7):c.-300G>C	rs80311039	0.00138
NM_014780.4(CUL7):c.-269A>G	rs377101095	0.00037
NM_014780.4(CUL7):c.-272C>T	rs754072990	0.00033
NM_014780.4(CUL7):c.-298C>G	rs369727378	0.00026
NM_014780.5(CUL7):c.-236G>A	rs886061423	0.00013
NM_014780.5(CUL7):c.-206A>G	rs1281399761	0.00008
NM_014780.5(CUL7):c.-186A>C	rs1159816166

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