List of variants in gene RET reported as likely benign for Renal hypodysplasia/aplasia 1

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: 35

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HGVS	dbSNP	gnomAD frequency
NM_020975.6(RET):c.337+9G>A	rs2435351	0.20641
NM_020975.6(RET):c.2071G>A (p.Gly691Ser)	rs1799939	0.16640
NM_020975.6(RET):c.*1969T>C	rs3026785	0.04255
NM_020975.6(RET):c.2508C>T (p.Ser836=)	rs1800862	0.03791
NM_020975.6(RET):c.1264-5C>T	rs9282835	0.02749
NM_020975.6(RET):c.2944C>T (p.Arg982Cys)	rs17158558	0.01567
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.*1742G>A	rs143369221	0.00349
NM_020975.6(RET):c.166C>A (p.Leu56Met)	rs145633958	0.00310
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.337+12G>A	rs200468424	0.00198
NM_020975.6(RET):c.2372A>T (p.Tyr791Phe)	rs77724903	0.00178
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.*576G>A	rs185408658	0.00044
NM_020975.6(RET):c.1946C>T (p.Ser649Leu)	rs148935214	0.00039
NM_020975.6(RET):c.2037C>T (p.Pro679=)	rs55862116	0.00039
NM_020975.6(RET):c.200G>A (p.Arg67His)	rs192489011	0.00036
NM_020975.6(RET):c.341G>A (p.Arg114His)	rs76397662	0.00029
NM_020975.6(RET):c.2088G>A (p.Ser696=)	rs150329150	0.00024
NM_020975.6(RET):c.874G>A (p.Val292Met)	rs34682185	0.00023
NM_020975.6(RET):c.1063+9G>A	rs765463636	0.00014
NM_020975.6(RET):c.1353G>T (p.Thr451=)	rs201568301	0.00010
NM_020975.6(RET):c.2418C>T (p.Tyr806=)	rs553418132	0.00005
NM_020975.6(RET):c.3188-9C>T	rs551159582	0.00005
NM_020975.6(RET):c.1118C>T (p.Ala373Val)	rs546866208	0.00004
NM_020975.6(RET):c.2976G>A (p.Pro992=)	rs528823385	0.00004
NM_020975.6(RET):c.*492G>C	rs568766449
NM_020975.6(RET):c.*499dup	rs201945709
NM_020975.6(RET):c.1523-7C>T	rs567967877

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