List of variants in gene RET reported as benign for digestive system disorder

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: 25

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HGVS	dbSNP	gnomAD frequency
NM_020975.6(RET):c.*1506G>A	rs2742241	0.83094
NM_020975.6(RET):c.1296A>G (p.Ala432=)	rs1800860	0.74268
NM_020975.6(RET):c.*1116T>C	rs2435355	0.22170
NM_020975.6(RET):c.2712C>G (p.Ser904=)	rs1800863	0.17043
NM_020975.6(RET):c.*388G>A	rs3026782	0.17032
NM_020975.6(RET):c.*95C>T	rs17028	0.16697
NM_020975.6(RET):c.*1591G>A	rs76759170	0.03751
NM_020975.6(RET):c.1264-5C>T	rs9282835	0.02749
NM_020975.6(RET):c.375C>A (p.Val125=)	rs1800859	0.00877
NM_020975.6(RET):c.*330A>G	rs141460872	0.00640
NM_020975.6(RET):c.*1870C>T	rs146771196	0.00539
NM_020975.6(RET):c.*1583G>A	rs192065891	0.00300
NM_020975.6(RET):c.*1599G>A	rs145954635	0.00265
NM_020975.6(RET):c.*1558A>C	rs142572876	0.00260
NM_020975.6(RET):c.1336G>C (p.Gly446Arg)	rs115423919	0.00238
NM_020975.6(RET):c.654G>A (p.Pro218=)	rs137928436	0.00138
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.*576G>A	rs185408658	0.00044
NM_020975.6(RET):c.2037C>T (p.Pro679=)	rs55862116	0.00039
NM_020975.6(RET):c.341G>A (p.Arg114His)	rs76397662	0.00029
NM_020975.6(RET):c.2976G>A (p.Pro992=)	rs528823385	0.00004
NM_020975.6(RET):c.2268C>T (p.Ala756=)	rs370791179	0.00001
NM_020975.6(RET):c.*1046G>C	rs143948954
NM_020975.6(RET):c.1523-7C>T	rs567967877

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