List of variants in gene RET reported as uncertain significance by CSER _CC_NCGL, University of Washington

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_020975.6(RET):c.785T>C (p.Val262Ala)	rs139790943	0.00024
NM_020975.6(RET):c.1531G>A (p.Glu511Lys)	rs201553718	0.00018
NM_020975.6(RET):c.2522C>T (p.Pro841Leu)	rs149891333	0.00015
NM_020975.6(RET):c.961G>A (p.Gly321Arg)	rs377767388	0.00009
NM_020975.6(RET):c.2081G>A (p.Arg694Gln)	rs141185224	0.00008
NM_020975.6(RET):c.1942G>A (p.Val648Ile)	rs77711105	0.00007
NM_020975.6(RET):c.3116C>T (p.Pro1039Leu)	rs79853121	0.00004
NM_020975.6(RET):c.2452G>A (p.Glu818Lys)	rs377767420	0.00003
NM_020975.6(RET):c.2656C>T (p.Arg886Trp)	rs146838520	0.00003
NM_020975.6(RET):c.539G>A (p.Arg180Gln)	rs370736139	0.00003
NM_020975.6(RET):c.1424G>A (p.Arg475Gln)	rs138624658	0.00002
NM_020975.6(RET):c.3191T>C (p.Met1064Thr)	rs149513065	0.00002

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