List of variants in gene combination LOC110121502, MCS+9.7, RET studied for not provided

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_020975.6(RET):c.73+9277T>C	rs2435357	0.79636
NM_020975.6(RET):c.73+9494A>C	rs2506004	0.78499
NM_020975.6(RET):c.73+9331A>G	rs73266201	0.02170
NM_020975.6(RET):c.73+9189C>A	rs73266197
NM_020975.6(RET):c.73+9189C>T	rs73266197
NM_020975.6(RET):c.73+9385_73+9395del	rs368137511

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