List of variants in gene GDNF reported as benign by Illumina Laboratory Services, Illumina

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: 20

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HGVS	dbSNP	gnomAD frequency
NM_000514.4(GDNF):c.*1605T>C	rs3749692	0.52136
NM_000514.4(GDNF):c.-51A>G	rs2973033	0.36519
NM_000514.4(GDNF):c.*2162G>T	rs17379771	0.29955
NM_000514.4(GDNF):c.*1651A>G	rs11111	0.22202
NM_000514.4(GDNF):c.*1264C>T	rs62360370	0.05866
NM_000514.4(GDNF):c.*2883G>A	rs77776214	0.04880
NM_000514.4(GDNF):c.*529G>A	rs58787312	0.04641
NM_000514.4(GDNF):c.*2204G>T	rs72745194	0.03446
NM_000514.4(GDNF):c.*1785G>T	rs115322727	0.02975
NM_000514.4(GDNF):c.*1141C>A	rs2972929	0.02126
NM_000514.4(GDNF):c.*1389A>G	rs78613670	0.01508
NM_000514.4(GDNF):c.*2713G>A	rs143311673	0.00725
NM_000514.4(GDNF):c.*363A>T	rs45611434	0.00554
NM_000514.4(GDNF):c.*450C>T	rs141395105	0.00496
NM_000514.4(GDNF):c.540A>G (p.Arg180=)	rs112417561	0.00329
NM_000514.4(GDNF):c.*1004T>C	rs79370077	0.00261
NM_000514.4(GDNF):c.*1541T>A	rs138502514	0.00209
NM_000514.4(GDNF):c.*1199A>T	rs77668737	0.00033
NM_000514.4(GDNF):c.*1898C>A	rs547628776	0.00006
NM_000514.4(GDNF):c.*2643C>T	rs146664109

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