Variants in gene RET with conflicting interpretations "benign" and "uncertain significance"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 14

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HGVS	dbSNP	gnomAD frequency
NM_020975.6(RET):c.2071G>A (p.Gly691Ser)	rs1799939	0.16640
NM_020975.6(RET):c.2944C>T (p.Arg982Cys)	rs17158558	0.01567
NM_020975.6(RET):c.166C>A (p.Leu56Met)	rs145633958	0.00310
NM_020975.6(RET):c.833C>A (p.Thr278Asn)	rs35118262	0.00056
NM_020975.6(RET):c.3112A>G (p.Thr1038Ala)	rs201740483	0.00047
NM_020975.6(RET):c.1946C>T (p.Ser649Leu)	rs148935214	0.00039
NM_020975.6(RET):c.200G>A (p.Arg67His)	rs192489011	0.00036
NM_020975.6(RET):c.874G>A (p.Val292Met)	rs34682185	0.00023
NM_020975.6(RET):c.2611G>A (p.Val871Ile)	rs145170911	0.00008
NM_020975.6(RET):c.3188-9C>T	rs551159582	0.00005
NM_020975.6(RET):c.539G>A (p.Arg180Gln)	rs370736139	0.00003
NM_020975.6(RET):c.1618A>G (p.Arg540Gly)	rs543376293	0.00001
NM_020975.6(RET):c.2538C>T (p.Leu846=)	rs201816539	0.00001
NM_020975.6(RET):c.3332C>T (p.Thr1111Met)	rs1003057639	0.00001

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