List of variants in gene RET reported as likely benign by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 23

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HGVS	dbSNP	gnomAD frequency
NM_020975.6(RET):c.1157C>T (p.Ala386Val)	rs115272158	0.00101
NM_020975.6(RET):c.1124T>A (p.Leu375Gln)	rs142338976	0.00066
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.1531G>A (p.Glu511Lys)	rs201553718	0.00018
NM_020975.6(RET):c.398G>A (p.Arg133His)	rs138265837	0.00012
NM_020975.6(RET):c.2601G>T (p.Glu867Asp)	rs141459368	0.00011
NM_020975.6(RET):c.337+11C>T	rs754967305	0.00011
NM_020975.6(RET):c.2611G>A (p.Val871Ile)	rs145170911	0.00009
NM_020975.6(RET):c.539G>A (p.Arg180Gln)	rs370736139	0.00003
NM_020975.6(RET):c.625+10G>A	rs371974705	0.00002
NM_020975.6(RET):c.777G>A (p.Pro259=)	rs1279646689	0.00002
NM_020975.6(RET):c.1386G>A (p.Ser462=)	rs587780807	0.00001
NM_020975.6(RET):c.1522+18G>A	rs763517546	0.00001
NM_020975.6(RET):c.342C>T (p.Arg114=)	rs143083395	0.00001
NM_020975.6(RET):c.108C>T (p.Tyr36=)	rs967553881
NM_020975.6(RET):c.1353G>A (p.Thr451=)	rs201568301
NM_020975.6(RET):c.2523G>A (p.Pro841=)	rs56195026
NM_020975.6(RET):c.3187+12C>T	rs897706317
NM_020975.6(RET):c.44TGC[8] (p.Leu19_Pro20insLeuLeuLeu)	rs768132465
NM_020975.6(RET):c.675G>C (p.Thr225=)	rs1837730338

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